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73505-32-5

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73505-32-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73505-32-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,5,0 and 5 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 73505-32:
(7*7)+(6*3)+(5*5)+(4*0)+(3*5)+(2*3)+(1*2)=115
115 % 10 = 5
So 73505-32-5 is a valid CAS Registry Number.
InChI:InChI=1/C45H78O/c1-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-34-46-39-30-32-44(5)38(35-39)26-27-40-42-29-28-41(37(4)25-23-24-36(2)3)45(42,6)33-31-43(40)44/h11-12,14-15,26,36-37,39-43H,7-10,13,16-25,27-35H2,1-6H3/b12-11-,15-14-/t37?,39-,40?,41+,42?,43?,44-,45+/m0/s1

73505-32-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (3S,10R,13R,17R)-10,13-dimethyl-17-(6-methylheptan-2-yl)-3-[(9Z,12Z)-octadeca-9,12-dienoxy]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene

1.2 Other means of identification

Product number -
Other names Cholest-5-ene,3-(9,12-octadecadienyloxy)-(3beta(9Z,12Z))

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:73505-32-5 SDS

73505-32-5Downstream Products

73505-32-5Relevant articles and documents

The Synthesis of Cholesteryl Alkyl Ethers

Halperin, G.,Gatt, S.

, p. 39 - 42 (2007/10/02)

Seventeen cholesteryl alkyl ethers were synthesized through alcoholysis of cholesterol p-toluenesulfonate.This method was found superior to the etherification of sodium or potassium cholesterylate with alkyl halides or methanesulfonates, especially for the preparation of long-chain unsaturated alkyl ethers of cholesterol of high specific activity.

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