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88247-66-9

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88247-66-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88247-66-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,2,4 and 7 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 88247-66:
(7*8)+(6*8)+(5*2)+(4*4)+(3*7)+(2*6)+(1*6)=169
169 % 10 = 9
So 88247-66-9 is a valid CAS Registry Number.

88247-66-9SDS

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 (24R,S)-24-phenylsulphonyl[26,27-2H6]cholest-5-ene-3β,25-diol 3-tetrahydropyran-2-yl ether

1.2 Other means of identification

Product number -
Other names -

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:88247-66-9 SDS

88247-66-9Relevant articles and documents

Synthesis of Cholesterol and Derivatives substituted in the Side chain

Kirk, David N.,Varley, Michael J.,Makin, Hugh L.J.,Trafford, David J.H.

, p. 2563 - 2567 (2007/10/02)

The carbanion derived from 24-phenylsulphonylchol-5-en-3β-ol 3-tetrahydropyranyl ether (6) reacted with acetone to give the 24-phenylsulphonyl-25-hydroxycholesterol derivative (7a), which was reduced by sodium amalgam to a separable mixture of the labelled 25-hydroxycholesterol and cholest-5,24-dien-3β-ol (desmosterol) derivatives. Cholesterol has been obtained via a selective reduction of the Δ24-unsaturation in desmosteryl benzoate with di-imide, or more efficiently by reducing 25-hydroxycholesteryl 3,25-diacetate w ith litium in ethylamine, without significant loss of label.The labelled 24,25-dihydroxycholesterols were also prepared from desmosteryl benzoate.

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