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Benzoic acid methyl ester benzoate

Methyl 4-hydroxy benzoate 4-hydroxy benzoic acid, methyl ester methyl p-hydroxybenzoate... [Pg.1060]

F.53) Benzoic acid, methyl ester, methyl benzoate (93-58-3] FEMA 2683... [Pg.181]

A13-00525 Benzoic acid, methyl ester CCRIS 5851 Clorius EINECS 202-259-7 Essence of niobe FEMA No, 2683 HSDB 5283 Methyl benzenecarboxylate Methyl benzoate Methylester kyseliny benzoove Niobe oil NSC 9394 Oil of niobe UN2938. Used in perfumery, as a solvent for cellulose esters and ethers, resins, rubber flavoring. Liquid mp = -15° bp = 199° d = 1.0933 insoluble in H2O, soluble in organic solvents Xm = 228,272,280 nm (s = 11000, 830, 686, MeOH) LDso (rat orl) n 1177 mg/kg. Lancaster Synthesis Co. Morflex Penta Mfg. Pentagon Chems. Ltd Sybron. [Pg.400]

Benzoic acid methyl ester. See Methyl benzoate Benzoic acid, 1-methylethyl ester. See Isopropyl benzoate... [Pg.445]

Benzoylacetyl. See 1-Phenyl-1,2-propanedione Benzoyl alcohol. See Benzyl alcohol Benzoylaminoacetic acid. See Hippuric acid o-(Benzoylamino) diphenyl disulfide. See 2,2 -Dibenzamidodiphenyl disulfide Benzoylbenzene. See Benzophenone 2-Benzoyl benzoic acid methyl ester o-Benzoylbenzoic acid methyl ester. See o-M ethyl benzoyl benzoate 4-Benzoylbiphenyl... [Pg.460]

Methylacetopyronone. See Dehydroacetic acid Methyl 12-acetoxy-9-octadecenoate Methyl 12-acetoxyoleate. See Methyl acetyl ricinoleate Methyl acetylacetate Methyl acetylacetonate. See Methyl acetoacetate Methyl acetylaminobenzoate CAS 2719-08-6 EINECS/ELINCS 220-318-5 Synonyms 2-(Acetylamino) benzoic acid, methyl ester Acetyl methyl anthranilate Acetyl-N-methyl anthranilate Methyl 2-(acetylamino) benzoate Methyl N-acetylanthranilate Empiricai C10H11NO3... [Pg.2575]

Synonyms Benzoic acid, 2-benzoyl-, methyl ester Benzoic acid, o-benzoyl-, methyl ester 2-Benzoyl benzoic acid methyl ester o-Benzoylbenzoic acid methyl ester MBB o-(Methoxycarbonyl) benzophenone Methyl 2-benzoylbenzoate Methyl o-benzoyl benzoate Empirical C15H12O3... [Pg.2590]

C8Hs02 93-58-3 Benzoic acid methyl ester see Methyl benzoate... [Pg.40]

The enzymatic process was carried out with a slurry of (E)-methyl 2-(3-(3-(2-(7-chloroquinolin-2-yl)vinyl)phaiyl)-3-oxopropyl)benzoate 79 (230kg) in a mixture of isopropyl alcohol (5 vol), toluene (1 vol), and triethanolamine buffer of pH 8.0 (3 vol). KRED CDX-026 (92kg) and the cofactor NADP-Na (023kg) were added to the reaction mixture, and the reaction was carried out at 40-45°C under stirring for 40-45h. From the reaction mixture, the crude (S)-2-[3-2[7-chloro-2-quinolinyl]ethenyl]phenyl-3-hydrox5q)ropyl] benzoic acid methyl ester 80 was obtained, which was purified by recrystallization to obtain pme product 80 as monohydrate 3 (233 kg, 97.2% yield, >99.9% ee) [109,110]. [Pg.89]

Fig. 5.1. A sample of floral scent compounds. (1) Substituted methyl esters of benzoic acid. The ester smells unpleasantly sweet when R = H (methyl benzoate), of wintergreen when R = OH (methyl salicylate), and of concord grape when R = NH2 (methyl anthranylate). Odorants with unusual origins and biological functions include the homoterpene 4,8-dimethyl-1,3,7-nonatriene (2) and the wet-earth compound geosmin (3). Some ubiquitous fragrance compounds are ben-zaldehyde (4), benzyl alcohol (5), indole (6), (S)-linalool (7), ( )-/ -ocimene (8), and of-farnesene (9). Fig. 5.1. A sample of floral scent compounds. (1) Substituted methyl esters of benzoic acid. The ester smells unpleasantly sweet when R = H (methyl benzoate), of wintergreen when R = OH (methyl salicylate), and of concord grape when R = NH2 (methyl anthranylate). Odorants with unusual origins and biological functions include the homoterpene 4,8-dimethyl-1,3,7-nonatriene (2) and the wet-earth compound geosmin (3). Some ubiquitous fragrance compounds are ben-zaldehyde (4), benzyl alcohol (5), indole (6), (S)-linalool (7), ( )-/ -ocimene (8), and of-farnesene (9).
CAS 606-45-1 EINECS/ELINCS 210-118-6 Synonyms o-Anisic acid, methyl ester Benzoic acid, 2-methoxy-, methyl ester Dimethyl salicylate 2-Methoxybenzoic acid methyl ester o-Methoxybenzoic acid methyl ester o-Methoxy methyl benzoate Methyl 2-methoxybenzoate Methyl o-methoxybenzoate Methyl salicylate o-methyl ester Empirical C9H10O3... [Pg.2584]

Synonyms o-Anisic acid, methyl ester Benzoic acid, 2-methoxy-, methyl ester Dimethyl salicylate o-Methoxybenzoic acid methyl ester o-M ethoxy methyl benzoate Methyl o-anisate Methyl 2-methoxybenzoate Methylsalicylate methyl ester Empiricai C9H10O3 Formuia CH3OC6H4CO2CH3 Properties M.w. 166.18 dens. 1.157 b.p. 248 C flash pt. > 230 F ref. index 1.5340 Toxicology LD50 (oral, rat) 3800 mg/kg, (skin, rabbit) > 5 g/kg mod. toxic by ing. si. toxic by skin contact TSCA listed Hazardous Decomp. Prods. Heated to decomp., emits acrid smoke and irritating vapors Uses Synthetic flavoring agent in foods and pharmaceuticals... [Pg.2654]

CAS 99-75-2 EINECS/ELINCS 202-784-1 Synonyms Benzoic acid, 4-methyl-, methyl ester p-Carbomethoxytoluene 4-(Methoxycarbonyl) toluene 4-Methylbenzoic acid methyl ester Methyl 4-methyl benzoate Methyl p-methylbenzoate Methyl 4-toluate MPT p-Toluic acid, methyl ester Empiricai C9H10O2... [Pg.2693]

Ethyl benzoate hydrogen chloride as a catalyst). Pass dry hydrogen chloride (Section 11,48,1) into a 600 ml. round-bottomed flask containing 116 g. (145 ml.) of absolute ethyl alcohol, cooled in an ice bath, until the increase in weight is 6 g. Add 30 g. of benzoic acid and reflux the mixture for 4 hours. Isolate the pure ester, b.p. 212-214°, as described for Methyl Benzoate. The yield is 32 g. [Pg.782]

Example 4.3. The p value for alkaline saponification of methyl esters of substituted benzoic acids is 2.38, and the rate constant for saponification of methyl benzoate under the conditions of interest is 2 x 10 s . Calculate the rate constant for the hydrolysis... [Pg.208]

Ethyl Benzoate.—This ester has not been found, so far, to occur naturally in essential oils. It has, however, been prepared by synthetic processes, for example, by condensing ethyl alcohol with benzoic acid by means of dry hydrochloric acid gas. Its odour is very similar to that of methyl benzoate (q.v.), but not quite so strong. It is an oil of specific gravity I OfilO, refractive index 1 5055, and boiling-point 213° at 745 mm. It is soluble in two volumes of 70 per cent, alcohol. [Pg.166]

A. Ethyl 4-Amino-3-(methylthiomethyl)benzoate [Benzoic acid, 4-amino-3-[(methylthio)methyl]-]. A 1-1., three-necked, round-bottomed flask is fitted with a mechanical stirrer, a condenser topped with a gas-inlet tube, and a two-neckcd adapter holding a low-temperature thermometer and a 100-ml., pressure-equalizing dropping funnel. The flask is charged with 10.50 g. (0.10 mole) of ethyl p-aminobenzoate [Benzocaine Benzoic acid, 4-amino-, ethyl ester] (Note 1), 300 ml. of acetonitrile, and 100 ml. of dichloromethane, is flushed with nitrogen, and is then immersed in a 40% aqueous methanol-dry ice bath maintained between... [Pg.15]

Methyl salicylate 144 (Structure 4.44), the main constituent of wintergreen oil, is derived from benzoic acid. Other important esters are linalyl acetate 145, benzyl benzoate 146 and benzyl isobutyrate 147. [Pg.65]

An optimised enzymatic synthesis of methyl benzoate in an organic medium was reported by Leszczak and Tran-Minh [43]. Methyl benzoate is part of the aroma of some exotic fruits and berries. The ester has been produced by direct esterification of benzoic acid with methanol in hexane/toluene catalysed by lipase from Candida rugosa. [Pg.492]

Increases in substrate levels that were accidentally produced by metabolic engineering also resulted in an olfaction-detectable increase in the methyl benzoate emission in transgenic carnation [30]. The metabolic flux from the anthocy-anin pathway was redirected towards benzoic acid, the methyl ester precursor, by antisense suppression of the flavanone 3-hydroxylase. [Pg.621]

Methyl benzoate, [93-58-3], CTfCOOCI Ig, bp, 198—200°C at 101.3 kPa d [ , 1.094 n], 1.5205. Insoluble in water, this is a colorless, transparent liquid solidifying at about 15°C. Methyl benzoate is prepared by the direct esterification of benzoic acid and methanol. It is used in the fragrance industry and in the production of other benzoate esters (via transesterification). A technical-grade methyl benzoate is available as a by-product in the manufacture of dimethyl terephthalate [120-61 -6]. [Pg.57]


See other pages where Benzoic acid methyl ester benzoate is mentioned: [Pg.3496]    [Pg.466]    [Pg.819]    [Pg.950]    [Pg.391]    [Pg.1066]    [Pg.533]    [Pg.256]    [Pg.1401]    [Pg.228]    [Pg.399]    [Pg.781]    [Pg.57]    [Pg.213]    [Pg.164]    [Pg.26]    [Pg.167]    [Pg.781]    [Pg.100]    [Pg.156]    [Pg.42]    [Pg.781]   


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Benzoate esters

Benzoic acid esters

Benzoic acid methyl ester

Benzoic acid, 3-methyl

Benzoic acid/benzoate

Benzoic esters

Benzoic methyl ester

Esters methyl benzoate

Methyl 2- benzoat

Methyl benzoate

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