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113806-26-1

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113806-26-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 113806-26-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,8,0 and 6 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 113806-26:
(8*1)+(7*1)+(6*3)+(5*8)+(4*0)+(3*6)+(2*2)+(1*6)=101
101 % 10 = 1
So 113806-26-1 is a valid CAS Registry Number.

113806-26-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-benzylidene-dl-alanine , sodium salt

1.2 Other means of identification

Product number -
Other names N-Benzyliden-dl-alanin, Natriumsalz

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:113806-26-1 SDS

113806-26-1Relevant articles and documents

A new direction in the reaction of α-iminocarboxylate salts with dialkyl chlorophosphites: Formation of bis[1-(dialkoxyphosphoryl)alkyl]amines

Dimukhametov, Mudaris N.,Musin, Rashid Z.,Buzykin, Boris I.,Latypov, Shamil K.,Mironov, Vladimir F.

, p. 40 - 42 (2005)

Sodium benzylidene-L-phenylglycinate and sodium benzylidene-D-alaninate react with dialkyl chlorophosphites and water contained in their crystal lattices to give stereoisomeric bis[1-(dialkoxyphosphoryl)alkyl]amines.

Versatile Stereoselective Synthesis of Completely Protected Trifunctional α-Methylated α-Amino Acids Starting from Alanine

Altmann, Eva,Nebel, Kurt,Mutter, Manfred

, p. 800 - 806 (2007/10/02)

A new route to completely protected α-methylated α-amino acids starting from alanine is described (see Scheme).These derivatives, which are obtained via base-catalyzed opening of the oxazolidinones (2S,4R)- and (2R,4S)-2, can be directly employed in pepti

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