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cholesteryl oleyl ether is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

66106-91-0

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66106-91-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66106-91-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,1,0 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 66106-91:
(7*6)+(6*6)+(5*1)+(4*0)+(3*6)+(2*9)+(1*1)=120
120 % 10 = 0
So 66106-91-0 is a valid CAS Registry Number.
InChI:InChI=1/C45H80O/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/h14-15,26,36-37,39-43H,7-13,16-25,27-35H2,1-6H3/b15-14-/t37-,39?,40+,41-,42+,43+,44+,45-/m1/s1

66106-91-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-3-[(E)-octadec-9-enoxy]-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 Cholesteryl oleyl ether

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:66106-91-0 SDS

66106-91-0Downstream Products

66106-91-0Relevant academic research and scientific papers

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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