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2-Azetidinecarboxylic acid, 1-(4-methoxyphenyl)-3-(1-methylethyl)-4-oxo-, methyl ester, (2S,3S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

216174-40-2

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216174-40-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 216174-40-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,6,1,7 and 4 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 216174-40:
(8*2)+(7*1)+(6*6)+(5*1)+(4*7)+(3*4)+(2*4)+(1*0)=112
112 % 10 = 2
So 216174-40-2 is a valid CAS Registry Number.

216174-40-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S,3S)-3-Isopropyl-1-(4-methoxy-phenyl)-4-oxo-azetidine-2-carboxylic acid methyl 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:216174-40-2 SDS

216174-40-2Downstream Products

216174-40-2Relevant academic research and scientific papers

The Direct Organocatalytic Asymmetric Mannich Reaction: Unmodified Aldehydes as Nucleophiles

Notz, Wolfgang,Tanaka, Fujie,Watanabe, Shin-Ichi,Chowdari, Naidu S.,Turner, James M.,Thayumanavan, Rajeswari,Barbas III, Carlos F.

, p. 9624 - 9634 (2007/10/03)

The unprecedented application of unmodified aldehydes as nucleophilic donors in direct catalytic asymmetric Mannich-type reactions is disclosed in a full account. Our efforts in broadening the applicability of chiral pyrrolidine-based catalysts in direct

A highly enantioselective route to either enantiomer of both α- and β-amino acid derivatives

Cordova, Armando,Watanabe, Shin-Ichi,Tanaka, Fujie,Notz, Wolfgang,Barbas III, Carlos F.

, p. 1866 - 1867 (2007/10/03)

This report describes the unprecedented use of unmodified aldehydes as donors in a catalytic asymmetric Mannich-type reaction. The proline-catalyzed reaction of N-PMP-protected α-imino ethyl glyoxylate with unmodified aliphatic aldehydes provided a genera

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