Welcome to LookChem.com Sign In|Join Free
  • or
Benzenepropanoic acid, a-methyl-3-nitro-, (S)-, also known as (S)-3-Nitro-α-methylbenzenepropanoic acid, is a chiral organic compound with the molecular formula C10H11NO4. It is a derivative of benzenepropanoic acid, featuring a methyl group at the α-position, a nitro group at the 3-position, and an (S)-configuration. Benzenepropanoic acid, a-methyl-3-nitro-, (S)- is of interest in the field of organic chemistry and pharmaceuticals, as it can be a precursor to various biologically active molecules. Its unique structure allows for potential applications in the synthesis of drugs and other chemical compounds, highlighting its importance in the development of new therapeutic agents.

138711-97-4

Post Buying Request

138711-97-4 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

138711-97-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138711-97-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,7,1 and 1 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 138711-97:
(8*1)+(7*3)+(6*8)+(5*7)+(4*1)+(3*1)+(2*9)+(1*7)=144
144 % 10 = 4
So 138711-97-4 is a valid CAS Registry Number.

138711-97-4SDS

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 (S)-(+)-2-(3-nitrobenzyl)propionic acid

1.2 Other means of identification

Product number -
Other names (S)-2-Methyl-3-(3-nitro-phenyl)-propionic acid

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:138711-97-4 SDS

138711-97-4Relevant academic research and scientific papers

CHEMOENZYMATIC SYNTHESIS OF THE ENANTIOMERS OF IOPANOIC ACID

Colombo, M.,Amici, M. De,Micheli, C. De,Pitre, D.,Carrea, G.,Riva, S.

, p. 1021 - 1030 (2007/10/02)

The two enantiomers of Iopanoic acid 1 were prepared in enantiomeric excess higher than 90percent by enzyme-catalyzed hydrolysis of precursors (+/-)-2a and (+/-)-3a, followed by standard chemical transformations.Among the tested enzymes, chymotrypsin and Lipase PS proved to be the most selective catalysts.The stereochemical outcome of the lipase-catalyzed hydrolyses of esters (+/-)-2a-d is strictly dependent upon both the size of the alkyl group attached to the chiral center and the substituent in the aromatic ring.The enantioselectivity of the reactions was evaluated by chiral HPLC and the configurations of the new products were assigned by chemical correlations.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 138711-97-4