Detail of "5542-60-9"

CAS Number:
5542-60-9
Name:
Propanoyl chloride,2-(4-chlorophenoxy)-2-methyl-
Molecular Structure:
Formula:
C₁₀H₁₀Cl₂O₂
Molecular Weight:
233.09
Synonyms:
Propionylchloride, 2-(p-chlorophenoxy)-2-methyl- (7CI,8CI);2-(4-Chlorophenoxy)-2-methylpropanoyl chloride;2-(4-Chlorophenoxy)-2-methylpropionyl chloride;2-(p-Chlorophenoxy)-2-methylpropionyl chloride;2-(p-Chlorophenoxy)isobutyrylchloride;Clofibric acid chloride;Clofibric chloride;a-(4-Chlorophenoxy)isobutyrylchloride;a-(p-Chlorophenoxy)-a-methylpropionyl chloride;a-(p-Chlorophenoxy)isobutyrylchloride;
Density:
1.271 g/cm³
Boiling Point:
284.074 °C at 760 mmHg
Flash Point:
112.489 °C

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2-(4-CHLOROPHENOXY)-2-METHYLPROPANOYL CHLORIDE

Supplier:Beijing Rexun Pharma (CRO) [ China (Mainland)]

925 Integral
925

Tel:86-10-59071915

Address:4A/F, Building A, Vantone Center, No.6 Jia, Chaoyangmenwai Avenue, Chaoyang District

670 Integral
670

Tel:+86-21-54096810

Address:No.2588,Jungong Road,Shanghai,China

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Erythromycin ester: Erythromycin ester. (Laboratorios Roger S. A., Spain). Belg. BE 833148 31 Dec 1975, 6 pp. (Unavailable). (Belgium). CODEN: BEXXAL. CLASS: IC: C07D. 5542-60-9 and 114-07-8 are also in the experiment. PRIORITY: ES 74-430061 14 Sep 1974. DOCUMENT TYPE: Patent CA Section: 33 (Carbohydrates) A monoester of erythromycin with 4-ClC6H4OCMe2CO2H was obtained by treating 7.34 g erythromycin with 2.32 g 4-ClC6H4OCMe2COCl. .

Synthesis of new antiatheromatic drugs: Synthesis of new antiatheromatic drugs. Study of the reactions esterification reactions of 5a-androstan-17b-ol-3-one.Some chemicals with cas registry numbers like 88674-61-7 and 5542-60-9 are also used. Volovel'skii, L. N.; Koryukina, V. N.; Popova, N. V.; Rastrepina, I. A.; Borozenets, L. K. (Khar'k. Nauchno-Issled. Inst. Endokrinol. Khim. Gorm., Kharkov, USSR). Khim. Prir. Soedin., (4), 473-6 (Russian) 1983. CODEN: KPSUAR. ISSN: 0023-1150. DOCUMENT TYPE: Journal CA Section: 32 (Steroids) Acylation of dihydrotestosterone by RCOCl (R = Et, 4-ClC6H4OCMe2) in pyridine gave mixts. of acyloxyandrostanones I and bis(acyoxy))androstenes II. Acid catalyzed hydrolysis of II gave I. .