1- Hydroxy-4-methylbenzene

SYNS 2-CRESOL o-CRESYLIC ACID 1-HYDROXY-2-METHYLBENZENE o-HYDROXYTOLUENE o-KRESOL (GERMAN) o-METHYLPHENOL 2-METHYLPHENOL ORTHOCRESOL o-OXYTOLUENE ORCRA WASTE NUMBER U052 o-TOLUOL... [Pg.391]

HYDROXYMETHYL)-l-AZA-3,7-DIOXABICYCLO(3.3.0)OCTANE see OMM300 1-HYDROXY-2-METHYLBENZENE see CNXOOO 1-HYDROXY-3-METHYLBENZENE see CNW750... [Pg.1725]

H.2) Phenol, 2-methyl-, 2-methylphenol, o-cresol, 1-hydroxy-2-methylbenzene, 2-hydroxytoluene, o-cresylic acid 95-48-7 FEMA 3480... [Pg.191]

Synonyms/Trade Names ortho-Cresol, 2-Cresol, o-Cresylic acid, 1-Hydroxy-2-methylbenzene, 2-Hydroxytoluene, 2-Methyl phenol ... [Pg.79]

CAS 95-48-7 EINECS/ELINCS 202-423-8 UN 2076 (DOT) FEMA 3480 Synonyms 2-Cresol o-Cresylic acid 1-Hydroxy-2-methylbenzene o-Hydroxytoluene 2-Methylphenol... [Pg.1082]

Flash vacuum pyrolysis of vicinal substituted hydroxy-methylbenzene thiols is used to obtain 2H,5H-benzo[, 2-b 4,5-b]-bisthiete (35) (60%) (94AG493). Similarly the thietes (36) and (37) are available from hydroxymethylnaphthalene thiols. Valence isomers of these thietes are thioquinone methides and examples of... [Pg.68]

Apart from the CH3 carbon at 22 <5/ppm, the remaining carbon-13 resonances in 3-hydroxy methylbenzene Fig. 11) are all in the unsaturated region between 100 and 160 <5/ppm. The 3-carbon is deshielded more than the remainder, being bonded directly to oxygen, but the chemical shifts of the remainder reflect the variations in electron density around the ring. [Pg.269]

Synonyms AI3-00075 Aptal Baktol Baktolan BRN 1237629 Candaseptic Caswell No. 185A CCRIS 1938 p-Chlor-/ 3-cresol Chlorocresol 4-Chlorocresol p-Chlorocresol 4-Chloro-/ 3-cresol 6-Chloro-/ 3-cresol 4-Chloro-l-hydroxy-3-methylbenzene 2-Chlorohydroxytoluene 2-Chloro-5-hydroxytoluene 4-Chloro-3-hydroxytoluene 6-Chloro-3-hydroxytoluene 4-Chloro-3-methyl-phenol /5-Chloro-3-methylphenol CMK EINECS 200-431-6 EPA pesticide chemical code 064206 3-Methyl-4-chlorophenol NSC 4146 Ottafact Parmetol Parol PCMC Peritonan Preventol CMK Raschit Raschit K Rasenanicon RCRA waste number U039 UN 2669. [Pg.285]

Synonyms AI3-00137 BRN 0506917 CCRIS 646 2-Cresol o-Cresol o-Cresylic acid EINECS 202-423-8 FEMA No. 3480 l-Hydroxy-2-methylbenzene 2-Hydroxytoluene o-Hydroxytoluene 2-Methylhydroxybenzene o-Methylhydroxybenzene o-Methylphenol o-Methylphenylol NSC 23076 Orthocresol o-Oxytoluene RCRA waste number U052 2-Toluol o-Toluol UN 2076. [Pg.798]

Synonyms AI3-00150 BRN 1305151 CCRIS 647 4-Cresol p-Cresol p-Cresylic acid EINECS 203-398-6 FEMA No. 2337 l-Hydroxy-4-methylbenzene p-Hydroxytoluene 4-Hydroxytoluene p-Kresol l-Methyl-4-hydroxybenzene 4-Methylhydroxybenzene p-Methyl-hydroxybenzene p-Methylphenol NSC 3696 4-Oxytoluene p-Oxytoluene Paracresol Paramethylphenol RCRA waste number U052 4-Toluol p-Toluol p-Tolyl alcohol UN 2076. [Pg.802]

Hydroxy 2 keto-4-methylpentane, see Diacetone alcohol Hydroxymethylbenzene, see Benzyl alcohol l-Hydroxy-2-methylbenzene, see 2-Methylphenol l-Hydroxy-4-methylbenzene, see 4-Methylphenol... [Pg.1491]

Bromophenylazo)-2/-toluene, 309 (2-BromophenyI)-iVM7-azoxy (2-hydroxy-5-methylbenzene), 358 p-Bromophenylurea, 138-139 Bromopropadiene, 17 2,3-Butadienoic add, 16 iV-l-Butenylpiperazine, 92 Butter yellow, hazard of, 291 f-Butylamine, oxidation of, 323 -Butyl azide, 269 f-Butyl-OlW-azoxymethane, 349 t-Butyl p-Bromophenylazoformate, 328 t-Butyl 2-(p-bromophenyl)carbazate, 328 H-Butyl carbamate, 238-239 t-Butyl carbamate, 241-243... [Pg.250]

BUTYLATED H T)ROXYTOLUENE BUTYLHYDRO-XYTOLUENE CAO 1 CAO 3 CATALIN CAO-3 CHEMANOX 11 DBMP DBPC (technical grade) DIBUTYLATED HYDROXYTOLUENE 2,6-DI-tert-BUTYL-p-CRESOL (OSHA, ACGIH) 2,6-DI-tert-BUTYL-1-HYDROXY-4-METHYLBENZENE 3,5-DI-tert-BUTYL-4-HYDROXYTOLUENE 2,6-DI-terc,BUTYL-p-KRESOL (CZECH) 2,6-DI-tert-BUTYL-p-METHYLPHENOL 2,6-DI-tert-BUTYL-4-METHYLPHENOL FEMANo. 2184 4-HYDROXY-3,5-DI-tert-BUTYLTOLUENE IMPRUVOL... [Pg.170]

BRONZE SCARLET 5-CHLORO-2-((2-HYDROXY-l-NAPHTHALENYL)AZO)-4-METHYLBENZENE SULFONIC ACID, BARIUM SALT (2 1) 5-CHLORO-2-((2-HYDROXY-l-NAPHTHALENYL)AZO)-4-METHYL-BENZENE SULPHONIC ACID, BARIUM SALT l-(4-CHLORO-o-SULFO-5-TOLYLAZO)-2-iNAPHTHOL,-BARIUM SALT C.I. PIGMENT RED COSMETIC CORAL RED KO BLUISH DAINTCHI LAKE RED C D C RED No. 9 DESERT RED ELJON LAKE RED C... [Pg.334]

SYNS 3-CRESOL m-CRESYLIC ACIDQ 1-HYDROXY-3-METHYLBENZENE O m-HYDROXY-TOLUENE m-KRESOL m-METHYLPHENOL 3-METHYLPHENOL m-OXYTOLUENE RCRA WASTE NUMBER U052 m-TOLUOL... [Pg.391]

SYNS 4-CRESOL p-CRESYLIC acid l-HYDROXY-4-METHYLBENZENE p-HYDROXYTOLUENE 4-HYDROXYTOLUENE p-KRESOL D l-METHYL-4-HYDROXYBENZENE p-METHYLPHENOL 4-METHYLPHENOL p-OXYTOLUENE PARAMETHYL PHENOL RCRA WASTE NUMBER U052 p-TOLUOL p-TOLYL ALCOHOL... [Pg.391]

HYDROXY-4-METHYLBENZENE see CNX250 4-(HYDROXYMETHYL)BENZENEDIAZONIUM TETRAFLUOROBORATE see HLX925... [Pg.1725]

Synonym m-cresylic acid, 1-hydroxy-3-methylbenzene, 3-hydroxytoluene, m-hydroxytoluene, 3-methylphenol, m-methy Iphenol, 3-cresol... [Pg.551]

Synonym p-cresylic acid, l-hydroxy-4-methylbenzene, 4-hydroxytoluene, 4-methylphenol, p-hydroxytoluene, p-methyl-phenol, 4-cresol... [Pg.560]

Aromatic substances, more than any other class of organic compounds, have acquired a large number of nonsystematic names. The use of such names is discouraged, but lUPAC rules allow for some of the more widely used ones to be retained (Table 15.1). rhus, methylbenzene is known commonly as toluene hydroxy benzene, as phenol aminobenzene, as aniline and so on. [Pg.517]

Aptal Baktol 4-chloro-m-cresol p-chloro-m-cresol 1-chloro-4-hydroxy-2-methylbenzene 2-chloro-5-hydroxytoluene 6-chloro-3-hydroxytoluene 4-chloro-3-methylphenol 3-methyl-4-chlorophenol Nipacide PC parachlorometacresol PCMC. [Pg.171]

In the case of the rhenium-catalyzed oxidation of methoxy- and hydroxy-substituted substrates, there is some complementary work concerning the general mechanism of the arene oxidation [10b, 11]. Since the major products in the oxidation of such arenes or phenols are the quinones, the formation of intermediary epoxides seems to be a predominant reaction step. When p-substituted phenols such as 2,6-di( -butyl)-4-methylphenol are treated with the MTO/H2O2 oxidant and acetic acid as solvent, the formation of hydroxydienones is observed. This is also reported for the oxidation using dimethyldioxirane as oxidant [20]. Since an arene oxide intermediate was postulated for the dioxirane oxidation, a similar mechanism is plausible here [11], e. g., for the oxidation of l,2,3-trimethoxy-5-methylbenzene (Scheme 3) or 2,6-di(f-butyl)-4-methyl-phenol. [Pg.438]

Nomenclature chaos in organic chemistry will not be ordered until a one-one correspondence between structure and name is restored. It was with this object specifically in view that a notational system (5) was devised which will generate a unique systematic name in every case. This does not, of course, mean (as some have supposed) that the sole and exclusive use of systematic names for organic substances is advocated. It would be pedantic to talk of hydroxybenzene or 4-hydroxy-l-methylbenzene when phenol or p-cresol is meant. But there must be an agreed, unique systematic or fiducial name for... [Pg.103]

Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...