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Cyclopropanecarboxylic acid, 1-[[(1,1-dimethylethoxy)carbonyl]amino]-2,3-diphenyl-, (2S,3S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

214557-96-7

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214557-96-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 214557-96-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,4,5,5 and 7 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 214557-96:
(8*2)+(7*1)+(6*4)+(5*5)+(4*5)+(3*7)+(2*9)+(1*6)=137
137 % 10 = 7
So 214557-96-7 is a valid CAS Registry Number.

214557-96-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S,3S)-1-(N-tert-butoxycarbonyl)amino-2,3-diphenyl-1-cyclopropanecarboxylic acid

1.2 Other means of identification

Product number -
Other names (2S,3S)-1-tert-Butoxycarbonylamino-2,3-diphenyl-cyclopropanecarboxylic 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:214557-96-7 SDS

214557-96-7Relevant academic research and scientific papers

Facile synthesis and highly efficient resolution of a constrained cyclopropane analogue of phenylalanine

Jiménez, Ana I,López, Pilar,Oliveros, Laureano,Cativiela, Carlos

, p. 6019 - 6026 (2007/10/03)

Enantiomerically pure (2R,3R)- and (2S,3S)-1-(N-tert-butoxycarbonyl)amino-2,3-diphenyl-1-cyclopropanecarboxylic acids have been prepared by HPLC resolution of a racemic precursor. The complete stereoselectivity of the cyclopropanation process, together wi

Conformational preferences of RNase A C-peptide derivatives containing a highly constrained analogue of phenylalanine

Moye-Sherman, Destardi,Jin, Song,Ham, Inhye,Lim, Dongyeol,Scholtz, J. Martin,Burgess, Kevin

, p. 9435 - 9443 (2007/10/03)

Both enantiomers of a highly constrained derivative of phenylalanine, FiFi, were prepared in optically pure form. Studies were performed to elucidate the effects of substituting this amino acid for phenylalanine in RN-24, a derivative of the RNase A C-pep

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