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109278-11-7

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109278-11-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 109278-11-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,2,7 and 8 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 109278-11:
(8*1)+(7*0)+(6*9)+(5*2)+(4*7)+(3*8)+(2*1)+(1*1)=127
127 % 10 = 7
So 109278-11-7 is a valid CAS Registry Number.

109278-11-7SDS

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 (S)-(+)-methyl 2-benzoylamino-3-(3,4-dimethoxyphenyl)propanoate

1.2 Other means of identification

Product number -
Other names .methyl (S)-2-benzamido-3-(3,4-dimethoxyphenyl)propanoate

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:109278-11-7 SDS

109278-11-7Relevant articles and documents

Practical enantioselective hydrogenation of α-aryl- and α-carboxyamidoethylenes by rhodium(I)-{1,2-bis[(o-tert-butoxyphenyl) (phenyl)phosphino]ethane}

Mohar, Barbara,Stephan, Michel

, p. 594 - 600 (2013)

The rhodium(I)-{1,2-bis[(o-tert-butoxyphenyl)(phenyl)phosphino]ethane} [Rh(I)-(t-Bu-SMS-Phos)] catalyst system displayed prime efficiency in the hydrogenation of large series of aamidostyrenes and a-amidoacrylates. Up to >99.9% enantiomeric excesses coupl

Process for producing threo-3-(3,4-dihydroxyphenyl)serine

-

, (2008/06/13)

Racemic or optically active threo-3-(3,4-dihydroxyphenyl)serine can be readily produced via a few short steps by a process involving the steps of reacting a racemic or optically active N-acyl DOPA derivative represented by the formula ?I!: STR1 wherein X

Optically Pure (S)-6,7-dimethoxy-1,2,3,4-tetrahydro-3-isoquinolinecarboxylic acid and asymmetric hydrogenation studies related to its preparation

O'Reilly,Derwin,Lin

, p. 550 - 556 (2007/10/02)

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