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A colorless liquid with a faint odor, commonly used as a building block in organic synthesis.

111138-65-9

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111138-65-9 Usage

Main applications

Production of pharmaceuticals, pesticides, and other chemical compounds.

Stereochemistry

The (2S-trans) designation indicates the stereochemistry of the molecule, which is important in determining its reactivity and interactions with other chemicals.

Use as a chiral auxiliary

It is used in asymmetric synthesis reactions to control the stereochemistry of the final product.

Check Digit Verification of cas no

The CAS Registry Mumber 111138-65-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,1,3 and 8 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 111138-65:
(8*1)+(7*1)+(6*1)+(5*1)+(4*3)+(3*8)+(2*6)+(1*5)=79
79 % 10 = 9
So 111138-65-9 is a valid CAS Registry Number.

111138-65-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S,5S)-5-(methoxycarbonyl)pyrrolidine-2-carboxylic acid

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:111138-65-9 SDS

111138-65-9Downstream Products

111138-65-9Relevant academic research and scientific papers

Organocatalytic, asymmetric, one-pot, three-component Mannich reaction of hydroxyacetone

Gu, Qing,Jiang, Ling-Xia,Yuan, Kui,Zhang, Lei,Wu, Xin-Yan

experimental part, p. 4198 - 4206 (2009/04/11)

The direct three-component asymmetric Mannich reactions of hydroxyacetone with anilines and aromatic aldehydes in the presence of (2S,5S)-5- (methoxycarbonyl)pyrrolidine-2-carboxylic acid afforded syn-1,2-amino alcohols in good-to-excellent yields (55~91%

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