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2-Azetidinecarboxylic acid, 1-[(4-methoxyphenyl)methyl]-2-(phenylmethyl)-, methyl ester, (2R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

681456-98-4

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681456-98-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 681456-98-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,8,1,4,5 and 6 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 681456-98:
(8*6)+(7*8)+(6*1)+(5*4)+(4*5)+(3*6)+(2*9)+(1*8)=194
194 % 10 = 4
So 681456-98-4 is a valid CAS Registry Number.

681456-98-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-methyl 1-(4-methoxybenzyl)-2-benzylazetidine-2-carboxylate

1.2 Other means of identification

Product number -
Other names (R)-2-Benzyl-1-(4-methoxy-benzyl)-azetidine-2-carboxylic acid methyl ester

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:681456-98-4 SDS

681456-98-4Downstream Products

681456-98-4Relevant academic research and scientific papers

Stereochemical diversity in asymmetric cyclization via memory of chirality

Kawabata, Takeo,Matsuda, Seiji,Kawakami, Shimpei,Monguchi, Daiki,Moriyama, Katsuhiko

, p. 15394 - 15395 (2007/10/03)

An enantiodivergent asymmetric cyclization of N-Boc-N-ω-bromoalkyl-α-amino acid derivatives has been developed. With potassium amide bases in DMF, cyclization proceeds with retention of configuration, while inversion of configuration was observed with lit

Simple access to novel azetidine-containing conformationally restricted amino acids by chemoselective reduction of β-lactams

Gerona-Navarro, Guillermo,Bonache, Ma. Angeles,Alías, Miriam,Pérez De Vega, Ma. Jesús,García-López, Ma. Teresa,López, Pilar,Cativiela, Carlos,González-Mu?iz, Rosario

, p. 2193 - 2196 (2007/10/03)

Reduction with diphenylsilane and catalytic amounts of tris(triphenylphosphine)rhodium(I) carbonyl hydride resulted in an efficient, chemoselective method for the transformation of amino-acid-derived β-lactams into the corresponding azetidines, which afte

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