
CAS Name: 2-Chloroethanol acetate
Percent Composition: C 39.20%, H 5.76%, Cl 28.93%, O 26.11%
Literature References: Prepn from ethylene oxide and acetyl chloride: E. L. Gustus, P. G. Stevens, J. Am. Chem. Soc. 55, 378 (1933). Physical properties: Ind. Eng. Chem. 32, 880 (1940).
CAS Name: 4,5-Dihydro-2-(1,2,3,4-tetrahydro-1-naphthalenyl)-1H-imidazole
Additional Names: 2-(1,2,3,4-tetrahydro-1-naphthyl)-2-imidazoline; tetryzoline
Percent Composition: C 77.96%, H 8.05%...
Literature References: Prepn from ethylenediamine, ethylenediamine hydrochloride, and methyl 1,2,3,4-tetrahydro-1-naphthoate: Synerholm et al., US 2731471 (1956 to Sahyun Labs.). Use as potentiator for veterinary depressants: Gardocki et al., US 2842478 (1958 to Pfizer).
CAS Name: (T-4)-Dihydrogen tetracarbonylferrate(2-)
Additional Names: iron hydrocarbonyl; iron tetracarbonyl dihydride
Percent Composition: C 28.28%, H 1.19%, Fe 32.87%, O 37.67%
Literature References: Prepn from Fe(CO)5: Blanchard, Coleman, Inorg. Synth. 2, 243 (1946); Sternberg et al., J. Am. Chem. Soc. 79, 6116 (1957); Bishop et al., J. Chem. Soc. 1959, 2484.
CAS Name: Formic acid phenylmethyl ester
Additional Names: formic acid benzyl ester
Percent Composition: C 70.57%, H 5.92%, O 23.50%
Literature References: Prepn from formic acid and benzyl alcohol: Mailhe, Chem. Ztg. 35, 508 (1911).
Additional Names: b-Naphthoquinoline; 5,6-benzoquinoline; naphthopyridine
Percent Composition: C 87.12%, H 5.06%, N 7.82%
Literature References: Prepn from from b-naphthylamine by the Skraup reaction: Knueppel, Ber. 29, 703 (1896); Clem, Hamilton, J. Am. Chem. Soc. 62, 2349 (1940); Uhle, Jacobs, J. Org. Chem. 10, 76 (1945).
CAS Name: (5a,20S)-20-Hydroxypregnan-3-one
Additional Names: 20a-hydroxy-5a-pregnan-3-one; 20a-hydroxy-3-oxo-5a-pregnane
Percent Composition: C 79.19%, H 10.76%, O 10.05%
Literature References: Prepn from funtumidine: Janot et al., Bull. Soc. Chim. Fr. 1960, 1669.
Additional Names: L-Glutamic acid g-ethyl ester; g-ethyl L-glutamate
Trademarks: Glutestere
Percent Composition: C 47.99%, H 7.48%, N 8.00%, O 36.53%
Literature References: Prepn from glutamic acid, ethanol, and hydrogen chloride: Hegedus, Helv. Chim. Acta 31, 737 (1948); Pravda, Collect. Czech. Chem. Commun. 24, 2083 (1959); CS 88344 (1959), C.A. 54, 8660h (1960).
CAS Name: (Phenylmethyl)carbamic acid 2-hydroxyethyl ester
Additional Names: benzylcarbamic acid 2-hydroxyethyl ester; 2-hydroxyethyl benzylcarbamate; glycol benzylcarbamateTrademarks: Hyamate ...
Literature References: Prepn from glycol cyclic carbonate and benzylamine: Viard, GB 689705 (1953 to Chauny Cirey).
CAS Name: 2,3,5,6-Tetrahydroxy-2,5-cyclohexadiene-1,4-dione
Additional Names: tetrahydroxy-p-benzoquinone; tetrahydroxyquinone; THQPercent Composition: C 41.88%, H 2.34%, O 55.78%
Literature References: Prepn from glyoxal: A. J. Fatiadi, W. F. Sager, Org. Synth. coll. vol. V, 1011 (1973). Clinical evaluation for ophthalmic fibrosis: R. Ching, Eye Ear Nose Throat Mon. 50, 101, 144 (1971).
CAS Name: 5-[(3,4,5-Trimethoxyphenyl)methyl]-2,4-pyrimidinediamine
Additional Names: 2,4-diamino-5-(3,4,5-trimethoxybenzyl)pyrimidine
Trademarks: Instalac (Virbac); Monotrim (Duphar); Prolop...
Literature References: Prepn from guanidine and b-ethoxy-3,4,5-trimethoxybenzylbenzalnitrile: Stenbuck, Hood, US 3049544 (1962 to Burroughs Wellcome); Hoffer, US 3341541 (1967 to Hoffmann-La Roche). Improved synthesis: B. Roth et al., J. Med. Chem. 23, 379, 535 (1980). Toxicity data: Yamamoto et al., Chemotherapy (Tokyo) 21, 187 (1973). Review: Burchall in Antibiotics vol. 3, J. W. Corcoran, F. E. Hahn, Eds. (Springer-Verlag, New York, 1975) pp 304-320. Comprehensive description: G. J. Manius, Anal. Profiles Drug Subs. 7, 445-475 (1978). Review of antibacterial activity, pharmacokinetics and therapeutic use: R. N. Brogden et al., Drugs 23, 405-430 (1982).
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