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DL-Norleucine, 6-hydroxy-, also known as 6-Hydroxy-DL-norleucine, is a synthetic amino acid derivative with the chemical formula C6H13NO3. It is a chiral molecule, meaning it has a non-superimposable mirror image, and is a racemic mixture of both the D and L isomers. DL-Norleucine, 6-hydroxy- is structurally similar to the naturally occurring amino acid leucine, but with an additional hydroxyl group (-OH) attached to the 6th carbon atom. DL-Norleucine, 6-hydroxy-, is primarily used in scientific research and pharmaceutical development, particularly in the study of protein synthesis and enzyme inhibition. Its unique structure allows it to interact with various biological systems, making it a valuable tool for understanding the mechanisms of amino acid metabolism and the development of potential therapeutic agents.

5462-80-6

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5462-80-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5462-80-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,6 and 2 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5462-80:
(6*5)+(5*4)+(4*6)+(3*2)+(2*8)+(1*0)=96
96 % 10 = 6
So 5462-80-6 is a valid CAS Registry Number.

5462-80-6SDS

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 .ε.-Hydroxy-DL-norleucine

1.2 Other means of identification

Product number -
Other names 2-amino-6-quinazolinol

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:5462-80-6 SDS

5462-80-6Relevant academic research and scientific papers

Mycobactins: Synthesis of (-)-Cobactin T from ε-Hydroxynorleucine

Maurer, Peter J.,Miller, Marvin J.

, p. 2835 - 2836 (2007/10/02)

The synthesis of (-)-cobactin T is described, the key step being ring closure between C6 and the hydroxamate N of α-N-(tert-butoxycarbonyl)-ε-hydroxynorleucine O-benzylhydroxamate.

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