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Dithiocarbonic acid O-(5α-cholestan-3β-yl) S-methyl ester is a complex organic compound with the chemical formula C29H51OS2. It is a derivative of dithiocarbonic acid, featuring a cholestan-3β-yl group attached to the oxygen atom and a methyl group attached to the sulfur atom. Dithiocarbonic acid O-(5α-cholestan-3β-yl) S-methyl ester is characterized by its unique structure, which includes a steroidal backbone with a sulfur-containing functional group. It is not commonly found in nature and is typically synthesized for specific applications in chemical research or as an intermediate in the synthesis of other compounds. Due to its specific structure, it may have potential applications in the fields of pharmaceuticals or materials science, although its exact uses and properties would depend on further research and development.

5211-17-6

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5211-17-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5211-17-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,1 and 1 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5211-17:
(6*5)+(5*2)+(4*1)+(3*1)+(2*1)+(1*7)=56
56 % 10 = 6
So 5211-17-6 is a valid CAS Registry Number.

5211-17-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3β-(methylthio)thiocarbonyloxy-5α-cholestane

1.2 Other means of identification

Product number -
Other names 3β,5α-cholestanyl xanthate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5211-17-6 SDS

5211-17-6Relevant academic research and scientific papers

13C NMR spectral assignment of five epimeric 3α- versus 3β-functionalized cholestane pairs

Ramos,Santos,Almeida,Motherwell,Costa

, p. 861 - 863 (2007/10/03)

13C NMR chemical shift assignments of five α- and β-epimeric pairs of cholestanes functionalized at C-3 are presented. Empirical increment estimations proved to be a valuable tool for the unequivocal structural elucidation when compared with th

Steroidal derived acids as inhibitors of human Cdc25A protein phosphatase

Peng, Hairuo,Xie, Wenge,Kim, Deog-Il,Zalkow, Leon H.,Powis, Garth,Otterness, Diane M.,Abraham, Robert T.

, p. 299 - 306 (2007/10/03)

A group of steroidal derived acids were synthesized and found to be human Cdc25A inhibitors. Their potency ranged from 1.1 to > 100 μM; the best ones compare very favorably with that of the novel cyano-containing 5,6-seco- cholesteryl acid 1 (IC50/s

Reduction et photoreduction de derives de l'acide carbonique influence de l'hexamethylphosphorotriamide

Dembele, Albert,Deshayes, Henri,Pete, Jean-Pierre

, p. 671 - 680 (2007/10/02)

Photoreduction and reduction of carbonic acid derivatives in HMPT have been compared.The highest yield of alkane was obtained from N,N-dimethylthiocarbamates either by the photochemical method or by reduction with a dissolved metal.Competitive reactions have been characterized: - during the photoreduction not only the alkane but products of a photo-Fries rearrangement and products of a homolytic cleavage were detected; - basic reactions can compete with the reduction of carbonic acid derivatives by sodium in HMPT.

ORGANOTELLURINIC ACID ANHYDRIDES AS SELECTIVE OXIDANTS IN ORGANIC SYNTHESIS

Barton, Derek H. R.,Finet, Jean-Pierre,Thomas, Martial

, p. 2319 - 2324 (2007/10/02)

Several aryltellurinic acid anhydrides have been compared for their oxidising properties in acetic acid.Very high yields of quinones and disulphides can be obtained under conditions where phenols are not oxidised.

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