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2665-02-3

2665-02-3

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  • [10,13-dimethyl-17-(6-methylheptan-2-yl)-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] 2,2,2-trifluoroacetate

    Cas No: 2665-02-3

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  • [10,13-dimethyl-17-(6-methylheptan-2-yl)-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] 2,2,2-trifluoroacetate cas 2665-02-3

    Cas No: 2665-02-3

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2665-02-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2665-02-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,6 and 5 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2665-02:
(6*2)+(5*6)+(4*6)+(3*5)+(2*0)+(1*2)=83
83 % 10 = 3
So 2665-02-3 is a valid CAS Registry Number.
InChI:InChI=1/C29H45F3O2/c1-18(2)7-6-8-19(3)23-11-12-24-22-10-9-20-17-21(34-26(33)29(30,31)32)13-15-27(20,4)25(22)14-16-28(23,24)5/h9,18-19,21-25H,6-8,10-17H2,1-5H3

2665-02-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

Product number -
Other names cholesteryl trifluoroacetate

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

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

More Details:2665-02-3 SDS

2665-02-3Downstream Products

2665-02-3Relevant articles and documents

Electrochemical synthesis of glycoconjugates of 3β-hydroxy- Δ5-steroids by using non-activated sugars and steroidal thioethers

Tomkiel, Aneta M.,Brzezinski, Krzysztof,?otowski, Zenon,Siergiejczyk, Leszek,Wa?ejko, Piotr,Witkowski, Stanis?aw,Kowalski, Jan,P?oszyn?ska, Jolanta,Sobkowiak, Andrzej,Morzycki, Jacek W.

, p. 8904 - 8913 (2013/09/23)

A new protocol for the electrochemical synthesis of glycoconjugates is presented. Thioether derivatives of cholesterol and other sterols were subjected to anodic oxidation in the presence of a sugar alcohol affording glycoconjugates with the sugar linked to a steroid moiety by an ether bond. The isomeric 6β-3α,5α-cyclo-steroidal thioethers proved to be better sterol donors than the normal 3β-Δ5-steroidal thioethers.

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