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Detail of "2867-93-8"

  • MSDS Download
  • CAS Number:
  • 2867-93-8
  • Name:
  • 3,5-Cyclocholestane,6-methoxy-, (3α,5R,6β)-

  • Molecular Structure:
  • Formula:
  • C28H48O
  • Molecular Weight:
  • 400.68
  • Synonyms:
  • 3α,5-Cyclo-5α-cholestane,6β-methoxy- (7CI,8CI);6β-Methoxy-3α,5-cyclo-5α-cholestane;NSC 134933;i-Cholesterol methyl ether;3,5-Cyclo-5α-cholestane, 6β-methoxy- (6CI);3,5-Cyclocholestane, 6-methoxy-, (3β,5α,6β)-;
  • Density:
  • 0.98 g/cm3
  • Boiling Point:
  • 436.2 °C at 760 mmHg
  • Flash Point:
  • 217.3 °C

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CAS No.2867-93-8 3,5-Cyclocholestane,6-methoxy-, (3α,5R,6β)-

C28H48O

Supplier:Guangzhou WeiBo Chemical Co., Ltd. [ China (Mainland)]

600Integral
600

Tel:020-33640779 32416961

Address:NO.1002-39,jinbi building,shijinshicha road,baiyun district,guanghzou city

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Reference

Microbial oxidation of sterol side-chains
Microbial oxidation of sterol side-chains. Bhattacharyya, P. K.; Rao, M. Krishna; Natarajan, Rama Devi; Ramgopal, Malathi; Madyastha, Prema; Madyastha, K. M. (Dep.There are some reagents like 57-88-5 is used in this study. Org. Chem., Indian Inst. Sci., Bangalore 560 012, India). J. Indian Chem. Soc., 61(1), 1-15 (English) 1984. CODEN: JICSAH. ISSN: 0019-4522. DOCUMENT TYPE: Journal CA Section: 16 (Fermentation and Bioindustrial Chemistry) Several sterol-metabolizing microorganisms, Pseudomonas convexa, P. stutzeri, Micrococcus species, Cephalosporium longisporum, and Moraxella species were isolated from soil. All oxidized the 8-C side chain of cholesterol [57-88-5]. The Moraxella was the most versatile as it degraded cholesterol derivs. such as 3b-methoxycholest-5-ene [1174-92-1], 3b-chlorocholest-5-ene [910-31-6], 3,5-cyclocholestan-6-one [7657-63-8], and K cholesteryl sulfate [6614-96-6] to the corresponding 17-keto steroids in 10-50% yield in shake flasks. It also gave high yields of estrone [53-16-7] from both 19-hydroxy-3b-acetoxycholest-5-ene [750-59-4] and 19-hydroxy-3b-acetoxysitost-5-ene [20835-78-3]. Two new enzymes one carrying out the oxidative O-demethylation of 6b-methoxy-3,5-cyclocholestane [2867-93-8] and the other, the isomerization of isosteroids to normal 3b-hydroxy-D6-steroids were discovered. Immobilized Moraxella cells in agar carried out the side chain degrdn. of cholesteryl sulfate [1256-86-6] to yield 3b-hydroxyandrost-5-en-17-one sulfate [651-48-9] and the 19-hydroxy-3b-acetoxy derivs. of both cholesterol and sitosterol to estrone in high yields. The half life of entrapped cells was estd. to be 28 days. .
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