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62234-37-1

62234-37-1

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62234-37-1 Usage

Chemical Properties

white to light yellow crystal powde

Uses

Nalpha-Benzyloxycarbonyl-D-2,3-diaminopropionic Acid

Check Digit Verification of cas no

The CAS Registry Mumber 62234-37-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,2,3 and 4 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 62234-37:
(7*6)+(6*2)+(5*2)+(4*3)+(3*4)+(2*3)+(1*7)=101
101 % 10 = 1
So 62234-37-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H14N2O4/c12-6-9(10(14)15)13-11(16)17-7-8-4-2-1-3-5-8/h1-5,9H,6-7,12H2,(H,13,16)(H,14,15)/t9-/m1/s1

62234-37-1 Well-known Company Product Price

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  • Aldrich

  • (96084)  Z-D-Dap-OH  ≥99.0% (NT)

  • 62234-37-1

  • 96084-1G

  • 2,588.04CNY

  • Detail

62234-37-1SDS

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 (R)-3-Amino-2-(((benzyloxy)carbonyl)amino)propanoic acid

1.2 Other means of identification

Product number -
Other names (2R)-3-amino-2-(phenylmethoxycarbonylamino)propanoic 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:62234-37-1 SDS

62234-37-1Relevant articles and documents

Synthesis of (R)- and (S)-2,3-diaminopropyl sulfate: Mechanism based inhibition of glutamate 1-semialdehyde aminomutase

Khayer, Khurshida,Jenn, Thierry,Akhtar, Mahmoud,John, Robert,Gani, David

, p. 1637 - 1641 (2007/10/03)

A short synthesis of each enantiomer of 2,3-diaminopropyl hydrogensulfate is described starting from (2R)- and (2S)-asparagine. The compounds serve as inhibitors for pyridoxal 5'-phosphate-dependent (2S)- glutamate 1-semialdehyde aminotransferase, a target for selective herbicides and antibacterial agents on the tetrapyrrole biosynthetic pathway. The (2R)- enantiomer, as predicted, serves as a potent irreversible inactivator. (C) 2000 Elsevier Science Ltd.

Substituted urido amino and imino acids and esters

-

, (2008/06/13)

Compounds of the formula STR1 wherein X is various imino or amino acids or esters are disclosed. These compounds possess angiotensin converting enzyme inhibition activity and depending upon the definition of X also possess enkephalinase inhibition activit

Conversion of serine to stereochemically pure β-substituted α-amino acids via β-lactones

Arnold,Kalantar,Vederas

, p. 7105 - 7109 (2007/10/02)

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