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56633-51-3

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  • (3S)-3-formamido-4-[[(2S)-1-hydroxy-1-oxo-3-phenylpropan-2-yl]amino]-4-oxobutanoic acid

    Cas No: 56633-51-3

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56633-51-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56633-51-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,6,3 and 3 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 56633-51:
(7*5)+(6*6)+(5*6)+(4*3)+(3*3)+(2*5)+(1*1)=133
133 % 10 = 3
So 56633-51-3 is a valid CAS Registry Number.

56633-51-3SDS

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-formyl-α-L-aspartyl-L-phenylalanine

1.2 Other means of identification

Product number -
Other names formyl-α-L-aspartyl-L-phenylalanine

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:56633-51-3 SDS

56633-51-3Relevant articles and documents

Process for the production of n-formyl-aspartyl-phenylalanine or its methyl ester

-

, (2008/06/13)

A process for producing N-formyl-aspartylphenylalanine or its methyl ester, wherein aspartic acid is reacted with formic acid and acetic anhydride in approximately stoichiometric quantities in the presence or absence of a catalyst and phenylalanine or its methyl ester is directly added to the dehydration mixture. This process has a higher yield of the desired N-formyl-dipeptide and minimizes the amount of by-products and unreacted starting materials.

Process for producing α-L-aspartyl-L-phenylalanine methyl ester

-

, (2008/06/13)

A process for preparing an α-L-aspartyl-L-phenylalanine methyl ester which comprises the steps of reacting formyl-L-aspartic anhydride with L-phenylalanine in the presence of water at a high pH, to produce formyl-α-L-aspartyl-L-phenylalanine; removing the formyl group from the formyl-α-L-aspartyl-L-phenylalanine and esterifying the resultant compound with methanol and hydrogen chloride to produce the hydrogen chloride salt of α-L-aspartyl-L-phenylalanine methyl ester; neutralizing the hydrogen chloride salt of α-L-aspartyl-L-phenylalanine methyl ester; and filtering the neutralized solution to produce α-L-aspartyl-L-phenylalanine methyl ester.

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