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7620-28-2

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7620-28-2 Usage

Chemical Properties

Solid

Uses

D-2-Aminoadipic Acid is a glutamine synthetase inhibitor.

Definition

ChEBI: An optically active form of 2-aminoadipic acid having D-configuration.

Check Digit Verification of cas no

The CAS Registry Mumber 7620-28-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,2 and 0 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7620-28:
(6*7)+(5*6)+(4*2)+(3*0)+(2*2)+(1*8)=92
92 % 10 = 2
So 7620-28-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H11NO4/c7-4(6(10)11)2-1-3-5(8)9/h4H,1-3,7H2,(H,8,9)(H,10,11)/t4-/m1/s1

7620-28-2 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
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  • Price
  • Detail
  • TCI America

  • (A2153)  D-2-Aminoadipic Acid  >95.0%(GC)(T)

  • 7620-28-2

  • 1g

  • 590.00CNY

  • Detail
  • TCI America

  • (A2153)  D-2-Aminoadipic Acid  >95.0%(GC)(T)

  • 7620-28-2

  • 5g

  • 1,990.00CNY

  • Detail
  • Alfa Aesar

  • (H27345)  D-2-Aminoadipic acid, 98%   

  • 7620-28-2

  • 250mg

  • 771.0CNY

  • Detail
  • Alfa Aesar

  • (H27345)  D-2-Aminoadipic acid, 98%   

  • 7620-28-2

  • 1g

  • 2381.0CNY

  • Detail
  • Alfa Aesar

  • (H27345)  D-2-Aminoadipic acid, 98%   

  • 7620-28-2

  • 5g

  • 7732.0CNY

  • Detail

7620-28-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name D-2-aminoadipic acid

1.2 Other means of identification

Product number -
Other names D-2-AMINOADIPIC ACID 98

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:7620-28-2 SDS

7620-28-2Relevant articles and documents

Preparation method of beta-homoglutamic acid

-

Paragraph 0022; 0033-0034, (2020/11/05)

The invention belongs to the field of preparation of organic compounds, and provides a preparation method of beta-homoglutamic acid. The method is characterized in that: 3-cyclohexenecarboxylic acid is used as a raw material, beta-homoglutamic acid is synthesized at a high yield through three the steps of reactions of Curtius rearrangement, olefin oxidation and protection group removal, and beta-homoglutamic acid with high yield and high optical purity can be obtained through configuration retention by using optically pure 3-cyclohexenecarboxylic acid. The method has the advantages of easily available raw materials, mild reaction conditions and low cost, and is suitable for large-scale preparation of beta-homoglutamic acid.

VITAMIN COMPRISING PYROLOQUINOLINE QUINONE AND USE THEREOF

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Page/Page column 20, (2008/06/13)

It is an object of the present invention to clarify the biochemical role of pyrroloquinoline quinone (PQQ) in living bodies by identifying an enzyme that uses PQQ as a coenzyme in mammals and then by clarifying the oxidation-reduction reaction, with which PQQ is associated as a coenzyme in living bodies. The present invention provides a method of using pyrroloquinoline quinone as a coenzyme for 2-aminoadipate 6-semialdehyde dehydrogenase.

TOTAL SYNTHESIS OF ENANTIOMERICALLY PURE D-α-AMINOADIPIC ACID

Amoroso, Rosa,Cardillo, Giuliana,Romero, Marta Susana,Tomasini, Claudia

, p. 75 - 78 (2007/10/02)

The diastereoselective cyclization of amidal (S,R)-2a, promoted by Hg(OTFA)2, afforded the imidazolidin-4-one (1'S,2R,5R)-3a as a single diastereoisomer. The subsequent transformation of the carbon-mercury bond and the acid hydrolysis of the heterocycle gave enantiomerically pure D-α-aminoadipic acid.

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