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103238-71-7

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103238-71-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103238-71-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,2,3 and 8 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 103238-71:
(8*1)+(7*0)+(6*3)+(5*2)+(4*3)+(3*8)+(2*7)+(1*1)=87
87 % 10 = 7
So 103238-71-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H11N3O7/c16-11(13-3-1-2-10(13)12(17)18)7-4-8(14(19)20)6-9(5-7)15(21)22/h4-6,10H,1-3H2,(H,17,18)/t10-/m0/s1

103238-71-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-1-(3,5-dinitrobenzoyl)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:103238-71-7 SDS

103238-71-7Downstream Products

103238-71-7Relevant articles and documents

Synthetic studies on L-proline and (4R)-hydroxy-L-proline derivatives

González, Teresa,Abad, Olga,Santano, M. Carmen,Minguillón, Cristina

, p. 1171 - 1182 (2007/10/03)

The preparation of a number of L-proline and (4R)-hydroxy-L-proline derivatives to assess their enantioselectivity when applied to several techniques and experimental conditions is described. All the derivatives prepared incorporated at least one 3,5-disubstituted aromatic ring that contained nitro, chloro or methyl groups and were obtained by classical methods. In spite of the difficulties that arise from the presence of rotational isomers in most cases, the compounds studied are fully described by their 1H and 13C NMR spectra.

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