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PENT-2-ENOIC ACID (2S,3S)-3-DIBENZYLAMINO-2-HYDROXYBUTYL ESTER is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

871948-97-9

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871948-97-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 871948-97-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,1,9,4 and 8 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 871948-97:
(8*8)+(7*7)+(6*1)+(5*9)+(4*4)+(3*8)+(2*9)+(1*7)=229
229 % 10 = 9
So 871948-97-9 is a valid CAS Registry Number.
InChI:InChI=1/C23H29NO3/c1-3-4-15-23(26)27-18-22(25)19(2)24(16-20-11-7-5-8-12-20)17-21-13-9-6-10-14-21/h4-15,19,22,25H,3,16-18H2,1-2H3/b15-4+/t19-,22+/m0/s1

871948-97-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name PENT-2-ENOIC ACID (2S,3S)-3-DIBENZYLAMINO-2-HYDROXYBUTYL ESTER

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:871948-97-9 SDS

871948-97-9Downstream Products

871948-97-9Relevant academic research and scientific papers

Total selective synthesis of enantiopure O1-acyl-3-aminoalkane- 1,2-diols by ring opening of aminoepoxides with carboxylic acids

Concellon, Jose M.,Suarez, Jose Ramon,Del Solar, Virginia,Llavona, Ricardo

, p. 10348 - 10353 (2005)

Synthesis of (2R,3S)- or (2S,3S)-O1-acyl-3-aminoalkane-1,2-diols by ring opening of enantiopure (2R,1′S)- or (2S,1′S)-2-(1- aminoalkyl)epoxides 1 or 2, with carboxylic acids in the presence of BF 3·Et2O and chlorotrimethyl

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