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CHOLESTERYL 2-ETHYLHEXANOATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

41329-01-5

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41329-01-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41329-01-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,3,2 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 41329-01:
(7*4)+(6*1)+(5*3)+(4*2)+(3*9)+(2*0)+(1*1)=85
85 % 10 = 5
So 41329-01-5 is a valid CAS Registry Number.
InChI:InChI=1/C35H60O2/c1-8-10-14-26(9-2)33(36)37-28-19-21-34(6)27(23-28)15-16-29-31-18-17-30(25(5)13-11-12-24(3)4)35(31,7)22-20-32(29)34/h15,24-26,28-32H,8-14,16-23H2,1-7H3/t25-,26+,28+,29+,30-,31+,32+,34+,35-/m1/s1

41329-01-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name Cholesteryl 2-ethylhexanoate

1.2 Other means of identification

Product number -
Other names [(3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] 2-ethylhexanoate

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:41329-01-5 SDS

41329-01-5Upstream product

41329-01-5Downstream Products

41329-01-5Relevant academic research and scientific papers

SYNTHESIS OF SOME NEW CHOLESTERYL ESTERS OF CHIRAL ALKANOIC ACIDS.

Gibson

, p. 43 - 53 (2007/10/05)

Six new cholesteryl esters have been prepared from chiral alkanoic acids. Oxidation of 2(S)-methylbutanol and 2(S)-ethyl-3-methybutyraldehyde gave the corresponding butyric acids, while condensation of the tosylates of the corresponding alcohols with diethyl malonate led ultimately to the substituted hexanoic acids. 2(R)-Methylpentanoic and ( minus )-2-ethylhexanoic acids were commercially available.

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