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17130-63-1

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17130-63-1 Usage

General Description

"(2Z)-2-(hydroxymethylidene)cholestan-3-one" is a chemical compound derived from cholesterol, with a molecular formula of C27H44O2. It is a ketone with a hydroxymethylidene substituent at the 2 position and an alkyl chain at the 3 position. (2Z)-2-(hydroxymethylidene)cholestan-3-one is believed to have potential biological activity, particularly in the fields of medicine and pharmacology, but further research is needed to fully understand its properties and potential applications.

Check Digit Verification of cas no

The CAS Registry Mumber 17130-63-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,1,3 and 0 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 17130-63:
(7*1)+(6*7)+(5*1)+(4*3)+(3*0)+(2*6)+(1*3)=81
81 % 10 = 1
So 17130-63-1 is a valid CAS Registry Number.

17130-63-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2Z)-2-(hydroxymethylidene)-10,13-dimethyl-17-(6-methylheptan-2-yl)-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-one

1.2 Other means of identification

Product number -
Other names 2-Hydroxymethylen-cholestanon-(3)

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:17130-63-1 SDS

17130-63-1Relevant articles and documents

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Ruzicka,Prelog,Battegay

, p. 1296,1300 (1948)

-

Synthesis and substance P receptor binding activity of androstano[3,2- b]pyrimido[1,2-a]benzimidazoles

Venepalli,Aimone,Appell,Bell,Dority,Goswami,Hall,Kumar,Lawrence,Logan,Scensny,Seelye,Tomczuk,Yanni

, p. 374 - 378 (2007/10/02)

Several heterosteroids containing a dihydroethisterone skeleton were prepared and shown to displace substance P in a receptor binding assay. Further biochemical (kinetic and Scatchard analyses) and pharmacological evaluation (substance P-induced plasma extravasation and salivation in the rat) of a representative example in this series (5a) established that these compounds are competitive antagonists at the substance P receptor.

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