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Glycine, N-[N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-valyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

142810-19-3

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  • [(2S)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-3-methylbutanamido]acetic acid

    Cas No: 142810-19-3

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142810-19-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 142810-19-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,8,1 and 0 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 142810-19:
(8*1)+(7*4)+(6*2)+(5*8)+(4*1)+(3*0)+(2*1)+(1*9)=103
103 % 10 = 3
So 142810-19-3 is a valid CAS Registry Number.

142810-19-3 Well-known Company Product Price

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  • Aldrich

  • (776556)  Fmoc-Val-Gly-OH  

  • 142810-19-3

  • 776556-500MG

  • 2,316.60CNY

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  • Aldrich

  • (776556)  Fmoc-Val-Gly-OH  

  • 142810-19-3

  • 776556-2.5G

  • 6,195.15CNY

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142810-19-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Fmoc-Val-Gly-OH

1.2 Other means of identification

Product number -
Other names FmocLG

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:142810-19-3 SDS

142810-19-3Upstream product

142810-19-3Downstream Products

142810-19-3Relevant articles and documents

Glutamic Acid Selective Chemical Cleavage of Peptide Bonds

Nalbone, Joseph M.,Lahankar, Neelam,Buissereth, Lyssa,Raj, Monika

supporting information, p. 1186 - 1189 (2016/03/15)

Site-specific hydrolysis of peptide bonds at glutamic acid under neutral aqueous conditions is reported. The method relies on the activation of the backbone amide chain at glutamic acid by the formation of a pyroglutamyl (pGlu) imide moiety. This activation increases the susceptibility of a peptide bond toward hydrolysis. The method is highly specific and demonstrates broad substrate scope including cleavage of various bioactive peptides with unnatural amino acid residues, which are unsuitable substrates for enzymatic hydrolysis.

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