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1963-21-9

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1963-21-9 Usage

Chemical Properties

white fine crystalline powder

Definition

ChEBI: A dipeptide formed from glycine and L-valine residues.

Check Digit Verification of cas no

The CAS Registry Mumber 1963-21-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,6 and 3 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1963-21:
(6*1)+(5*9)+(4*6)+(3*3)+(2*2)+(1*1)=89
89 % 10 = 9
So 1963-21-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H14N2O3/c1-4(2)6(7(11)12)9-5(10)3-8/h4,6H,3,8H2,1-2H3,(H,9,10)(H,11,12)/t6-/m0/s1

1963-21-9 Well-known Company Product Price

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  • TCI America

  • (G0148)  Glycyl-L-valine  >99.0%(T)

  • 1963-21-9

  • 1g

  • 485.00CNY

  • Detail
  • TCI America

  • (G0148)  Glycyl-L-valine  >99.0%(T)

  • 1963-21-9

  • 5g

  • 1,140.00CNY

  • Detail

1963-21-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name Glycyl-L-valine

1.2 Other means of identification

Product number -
Other names Gly-L-val

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:1963-21-9 SDS

1963-21-9Relevant articles and documents

-

Katakai,R. et al.

, p. 327 - 329 (1972)

-

Synthesis of dendritic oligo(aryl sulfone)s as supports for synthesis

Taylor, Paul C.,Wall, Michael D.,Woodward, Peter R.

, p. 12314 - 12322 (2007/10/03)

A short, divergent route to G1 oligo(aryl sulfone)s and a G 2 oligo(aryl sulfone) dendrimer using nucleophilic aromatic substitution reactions is described. A range of tetrasubstituted pentasulfones are proposed for applications as homogeneous supports for synthesis. Key to achieving selectivity in the syntheses is the activation of leaving groups by sulfide to sulfone oxidation. Preparation of the G2 oligo(aryl sulfone) is low-yielding due to competition from SET processes that are interesting from a mechanistic point of view. The utility of the supports is exemplified with a four step synthesis of a dipeptide and by 'react and release' synthesis of amides.

Polypeptide, DNA fragment encoding the same, drug composition containing the same and process for producing the same

-

, (2008/06/13)

This invention particularly provides a novel polypeptide having high protease-inhibiting activity, preferably FXa-inhibiting activity, which comprises, at least as a part of the polypeptide, an amino acid sequence resulting from substitution of an amino acid for at least one amino acid in the following amino acid sequence (1), wherein the amino acid substitution is at least one substitution selected from the following substitution means (i) to (iii). It also provides a process for the production of the polypeptide, a novel DNA fragment encoding the polypeptide and a drug composition containing the same. Amino acid sequence (1) STR1 (i) Substitution of 15 position Gln counting from the N-terminus by an amino acid other than Gln. (ii) Substitution of 42 position Tyr counting from the N-terminus by an amino acid other than Tyr. (iii) Substitution of 7 position Arg counting from the N-terminus by an amino acid other than Arg.

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