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Phenylic acid

Phenyl-jodidchlorid, n. phenyl iodochloride, -milchsaure, /. phenyllactic acid, -saure, /. phenylic acid (phenol, CeHaOH). -schwefel-saure, /. phenylsulfuric acid, -senfol, n. phenyl mustard oil. -siliciumchlorid, n. trichlorophenylsilane, CaHiSiCla. -verbindung, /. phenyl compound, -wasserstoff, m. phenyl hydride, benzene. [Pg.339]

Synonym(s) Benzenol, hydroxybenzene, monophenol, oxybenzene, phenyl alcohol, phenyl hydrate, phenyl hydroxide, phenylic acid, phenylic alcohol Lewis 1996... [Pg.156]

Synonyms AI3-01814 AIDS-352 Baker s P and S liquid and ointment Benzenol BRN 0969616 Carbolic acid Carbolic oil Caswell No. 649 CCRIS 504 CRS EINECS 203-632-7 EPA pesticide chemical code 064001 FEMA No. 3223 Fenosmolin Fenosmoline Hydroxy-benzene IPH Izal Monohydroxybenzene Monophenol NA 2821 NCI-C50124 NSC 36808 Oxybenzene Phenic acid Phenic alcohol Phenol alcohol Phenyl hydrate Phenyl hydroxide Phenylic acid Phenylic alcohol RCRA waste number U188 UN 1671 UN 2312 UN 2821. [Pg.949]

Phenyl hydrate, see Phenol Phenyl hydride, see Benzene Phenyl hydroxide, see Phenol Phenylic acid, see Phenol Phenylic alcohol, see Phenol Phenylmethane, see Toluene Phenyl methanol, see Benzyl alcohol Phenyl methyl alcohol, see Benzyl alcohol iV-Phenylmethylamine, see Methylaniline... [Pg.1505]

Synonyms Carbolic acid phenic acid phenylic acid phenyl hydroxide hydroxyben-zene oxybenzene... [Pg.568]

Attempts to rearrange tne phenyl acid into the trane form by heating to 290° with fused alkali yielded a small amount of an isomeric acid. Tnis acid was unattacked by potassium permanganate and was probably the cls-phenyl cls-trans dlcarboxyllc acid not enough was at hand to Investigate its properties. [Pg.27]

Garton, Robinson and Williams66 have studied the rate of acid hydrolysis of phenyl D-glucosiduronic acid as compared with phenyl acid sulfate. The ester acid sulfate was hydrolyzed completely by N hydrochloric acid at 93-95° in 10 minutes, 50 times as rapidly as the D-glucosiduronic acid. After 20 minutes, only 40% of the latter was hydrolyzed. On refluxing... [Pg.199]

By increasing the temperature over > 300°C, the phenyl glycidic acid esters are converted to phenyl acid esters. That occurs in a consecutive decarbonylation of a-ketone carboxylic acid esters as intermediate. In the case of p-tert-butyl glycidic acid ester in the presence of a boron-pentasil zeolite at 350 °C the ratio between a-ketone carboxylic acid ester and the phenyl acetic acid ester is 65 35. [Pg.305]

SYNS ACIDE CARBOLIQUE (FRENCH) BAKER S P AND S LIQUID and OINTMENT BENZENOL CARBOLIC ACID CARBOLSAEURE (GERMAN) FENOL PUTCH, POLISH) FENOLO (ITALIAN) H T)ROXYBENZENE MONOHYDROXYBENZENE MONOPHENOL NCI-C50124 OXYBENZENE PHENIC ACID PHENOL, molten pOT) PHENOL ALCOHOL PHENOLE (GERMAN) PHENYL HYDRATE PHENYL HYDROXIDE PHENYLIC ACID PHENYLIC ALCOHOL RCRA WASTE NUMBER U188... [Pg.1093]

PHENYL-l-HYDROXYPENTANE see BQJ500 PHENYLIC ACID see PDN750... [Pg.1837]

Synonym carbolic acid, phenic acid, phenylic acid, phenyl hydrate, phenyl hydroxide, hydroxybenzene, oxybenzene Chemical Name phenol CAS Registry No 108-95-2 Molecular Formula C HjOH Molecular Weight 94.111 Melting Point (°C) ... [Pg.529]

Octyl phenyl acid phosphate Albright Wilson... [Pg.662]

Carbolic acid hydroxybenzene oxybenzene phenic acid phenyl hydrate phenyl hydroxide phenylic acid phenylic alcohol. [Pg.514]

Phenylation of anions. The reagent phenylates acidic di- and tri-ketones in good yield. r-Butanol is the preferred solvent and sodium is used to generate the anion. A radical mechanism is proposed. [Pg.904]

Phenol (carbolic acid phenylic acid benzophenol hydroxybenzene). [Pg.968]

Armstrong et al. (All, A14) have found the following 3-hydroxy-phenyl acids in normal human urine m-hydroxy-benzoic, -hippuric, -phenylacetic, -phenylpropionic, and -phenylhydracrylic (Fig. 9). [Pg.80]

The enzyme found by Axelrod (A20) to be responsible for 0-meth-ylation of the catechols, namely, catechol-O-methyltransferase, plays a fundamental role in the biological synthesis of the 3-methoxy-4-hydroxy-phenyl acids. [Pg.84]

PHENYLIC ACID (108-95-2) C HjOH Combustible solid, smelt (molten), or liquid [explosion limits in air (% by volume when heated) 3 to 10 flash point 174°F/79°C autoignition temp 1319°F/715°C Fire Rating 2]. Violent reaction with butadiene, strong oxidizers. Reacts, possibly violently, with strong acids caustics, aliphatic amines amides, oxidizers, calcium hypochlorite formaldehyde, lead diacetate menthol, P-naphthol, peroxydisulfuric acid peroxymonosulfuric acid potassium hydroxide sodium nitrite 1,2,3-trihydroxybenzene. Liquid attacks some plastics, rubber and coatings hot liquid attacks aluminum, magnesium, lead, and zinc. On small fires, use CO2 or dry chemical extinguishers. [Pg.856]


See other pages where Phenylic acid is mentioned: [Pg.658]    [Pg.908]    [Pg.934]    [Pg.705]    [Pg.513]    [Pg.286]    [Pg.13]    [Pg.658]    [Pg.27]    [Pg.658]    [Pg.908]    [Pg.38]    [Pg.124]    [Pg.27]    [Pg.27]    [Pg.16]    [Pg.663]    [Pg.706]    [Pg.965]    [Pg.896]    [Pg.658]    [Pg.908]    [Pg.976]    [Pg.124]    [Pg.81]    [Pg.247]   
See also in sourсe #XX -- [ Pg.568 ]

See also in sourсe #XX -- [ Pg.514 ]

See also in sourсe #XX -- [ Pg.230 ]




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1- Hydroxy-4-phenyl-5-carboxylic acid

1-Phenyl-1,2,3-triazole-4-carboxylic acid

1.3.4- Oxadiazole-2-acetic acid, 5-phenyl

2,4-Hexadienedioic acid, 3-methyl-4-phenyl

2,4-Hexadienedioic acid, 3-methyl-4-phenyl dimethyl ester, cobalt complex

2-Phenyl butyric acid

2-Propenoic acid, 3-phenyl

2-Propenoic acid, 3-phenyl-, methyl ester

2-Propynoic acid, 3-phenyl-, methyl ester cobalt complex

2-Propynoic acid, phenyl-, methyl ester

2-bromobenzenesulfonic acid phenyl esters

2-phenyl-4-oxazolecarboxylic acid methyl ester

2.2- Dichloro-acetic acid phenyl ester

2.2- dimethyl-3-phenyl-cyclopropane carboxylic acid

2.4- Dimethyl phenyl acetic acid

3- Phenyl-3-hydroxypropanoic acid

3- Phenyl-4,5-pyridazinedicarboxylic acid

3- Phenyl-4-pentenoic acid

3- Phenyl-propionic acid

3- amino-9-methoxy-2,6,8-trimethyl-1 phenyl-4,6-decadienoic acid

3-Phenyl-2-bromo-2-propen acid

3-Phenyl-3-bromopropan acid

3-Phenyl-propionic acid acidity constant

4-Phenyl-3-butenoic acid

5- Phenyl-pentanoic acid

5- phenyl valeric acid

7-methoxy-2-phenyl- -perchlorate perchloric acid

A-Phenyl propionic acid

A-Phenyl-2-piperidineacetic acid

Acetic acid, 2,4,6-Trimethyl-phenyl

Acetic acid, 3,4-dimethoxy-phenyl

Acetic acid, trifluoro-, phenyl ester

Acid Esters From Phenols Phenyl Cyanate

Acids phenyl boronic acid synthesis

Alkylsulfonic acid phenyl ester

Amino Acids phenyl bearing

Amino acid derivatives, 3-phenyl-2-thiohydantoin

Amino phenyl propiolic acid

Aryloxy-p-Phenyl Propionic Acids

Asymmetric hydrogenation of vinylphosphonic acids carrying a phenyl substituent at

B-NOD (2-Hydroxy-benzoid acid 3-nitrooxymethyl-phenyl ester)

Benzeneacetic acid, a-phenyl

Benzoic acid, phenyl ester

Biguanide-/>-sulfonic acid, 1-phenyl

Boric acid phenyl borate

Butyric acid, «,7-dicyano-<»-phenyl

Butyric acid, «,7-dicyano-<»-phenyl ETHYL ESTER

CYANIC ACID, PHENYL ESTER

Carbamic acid phenyl ester

Carboxylic acid phenyl ester

Cinnamic acid, 2,3-dimethoxy a-PHENYL

Cinnamic acid, 2-phenyl

Dichloroacetic acid phenyl

FORMIMIDIC ACID, N-PHENYL-, ETHYL

Fatty acid phenyl esters

Fatty acid phenyl-substituted

Formic acid phenyl ester

Formimidic acid, N-phenyl-, ethyl ester

GlutariC acid 3-METHYL-3-PHENYL

Glycidic acid, /3-methyl- -phenyl

Glycidic acid, /3-methyl- -phenyl ETHYL ESTER

Glyoxylic acid methyl phenyl ester

Glyoxylic acid, phenyl

Hexanoic acid, 2-phenyl-2-methylSchmidt reaction

Hippuric acid, phenyl ester

Hydrolysis, amide to acid and decarboxylation of a-phenyl-acarbethoxyglutaronitrile

Hydroxy aldehydes phenyl acetic acid

Hydroxybenzoic acid phenyl ester

Isocyanic acid, phenyl ester

Methyl-phenyl-carbamic acid

Methyl-phenyl-carbamic acid ethyl ester

Monocarboxylic acids phenyl-substituted

Nitro, acids phenyl acetic acid

Nitro, acids phenyl propiolic acid

Octyl-phenyl acid phosphate

Phenic acid phenyl hydroxide

Phenyl Boronic Acid Synthesis (Clariant)

Phenyl Boronic Acid Synthesis (Scheme

Phenyl C61-butyric acid methyl ester

Phenyl Hydroxamic Acids

Phenyl Phenylazobenzoic acid

Phenyl Succinic Acid

Phenyl acetic acid, 4-nitro

Phenyl acid catalyzed

Phenyl acid phosphate

Phenyl acid phosphate reagent

Phenyl acrylic acid

Phenyl arsonic acid

Phenyl carboxylic acid

Phenyl crotonic acid

Phenyl esters of benzoic acid

Phenyl ethyl barbituric acid

Phenyl ethyl malonic acid diethyl ester

Phenyl formic acid

Phenyl glycine ortho-carboxylic acid

Phenyl glycolic acid

Phenyl group Phosphoric acid

Phenyl hydrazine sulfonic acid

Phenyl hydroxy acetic acid

Phenyl isothiocyanate acid determination

Phenyl maleic acid

Phenyl malonic acid

Phenyl methanoic acid

Phenyl methylphosphonic acid

Phenyl phosphonic acid

Phenyl phosphoric acid

Phenyl salicylic acid

Phenyl sulfuric acid , potassium salt

Phenyl, propiolic acid

Phenyl- hydroxyacetic acid

Phenyl-1,4-diboronic acid

Phenyl-2-propenoic acid phenylmethyl ester

Phenyl-4,6-decadienoic acid

Phenyl-C61-butyric acid methyl ester PCBM)

Phenyl-C6i-butyric acid methyl ester

Phenyl-C6i-butyric acid methyl ester PCBM)

Phenyl-Cgi-butyric acid methyl ester (PCBM

Phenyl-acetic acid

Phenyl-acetic acid acetate

Phenyl-acetic acid acidity constant

Phenyl-acetic acid aldehyde

Phenyl-acetic acid carbinol

Phenyl-acetic acid cinnamate

Phenyl-acetic acid esters

Phenyl-acetic acid ether

Phenyl-acetic acid ethylene

Phenyl-acetic acid isothiocyanate

Phenyl-acetic acid propionate

Phenyl-boronic acid

Phenyl-carbamic acid ethyl ester

Phenyl-glycidic acid

Phenyl-lactic acid

Phenylcarbamic acid phenyl ester

Phosphinic acid, phenyl-, ethyl ester

Phosphonic acid, phenyl-, diethyl ester

Phosphonous acid, phenyl-, dimethyl ester

Phosphonous acid, phenyl-, dimethyl ester nickel complex

Phosphoric acid diethyl phenyl

Phosphoric acid phenyl ester

Preparation of Phenyl-glycidic Acids

Propanethioic acid S-phenyl ester

Propionic acid, 2-phenyl-2- synthesis

Propionic acid, 2-phenyl-2- synthesis via arene-metal complex

Propionic acid, 3-Hydroxy-2-phenyl

Pyridine-2-carboxylic acid phenyl ester

Pyruvate/pyruvic acid phenyl

Salicylic acid phenyl ester

Succinic acid, -benzhydrylidene PHENYL

Succinic acid, o-benzhydrylidene PHENYL

Suzuki with phenyl boronic acid

Synthesis phenyl boronic acid

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