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63088-04-0

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63088-04-0 Usage

Uses

A highly selective and potent agonist for kainate receptors.

Check Digit Verification of cas no

The CAS Registry Mumber 63088-04-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,0,8 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 63088-04:
(7*6)+(6*3)+(5*0)+(4*8)+(3*8)+(2*0)+(1*4)=120
120 % 10 = 0
So 63088-04-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H11NO4/c1-3(2-4(8)9)5(7)6(10)11/h3,5H,2,7H2,1H3,(H,8,9)(H,10,11)/t3-,5+/m1/s1

63088-04-0 Well-known Company Product Price

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  • Sigma

  • (T2455)  T3MG  

  • 63088-04-0

  • T2455-5MG

  • 1,443.78CNY

  • Detail
  • Sigma

  • (T2455)  T3MG  

  • 63088-04-0

  • T2455-25MG

  • 5,819.58CNY

  • Detail

63088-04-0SDS

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 (+/-)-threo-3-Methylglutamic Acid

1.2 Other means of identification

Product number -
Other names (±)-threo-3-Methylglutamic acid

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:63088-04-0 SDS

63088-04-0Relevant articles and documents

threo-Selective Michael Addition of N,N-Dibenzylglycinate and Alaninate Enolates to α,β-Unsaturated Esters. A Concise and Stereoselective Synthesis of (+/-)-CCG-II

Yamaguchi, Masahiko,Torisu, Kazuhiko,Minami, Toru

, p. 377 - 380 (2007/10/02)

Lithium enolates of N,N-dibenzylglycinate and alaninate added to β-substituted α,β-unsaturated esters, and threo-adducts were obtained in high stereoselectivities.The reaction was employed in a concise and stereoselective synthesis of (+/-)-CCG-II.

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