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4379-13-9

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4379-13-9 Usage

General Description

L-Isoleucinol hydrochloride is a chemical compound that is a derivative of the amino acid isoleucine. It is commonly used in the production of pharmaceuticals, as well as in the synthesis of various organic compounds. L-Isoleucinol hydrochloride has been found to exhibit antibacterial and antifungal properties, making it potentially useful in the development of antimicrobial agents. Additionally, it is also used as a chiral building block in the preparation of chiral drugs and pharmaceuticals. Overall, L-Isoleucinol hydrochloride is a versatile chemical with various potential applications in pharmaceutical and organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 4379-13-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,7 and 9 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4379-13:
(6*4)+(5*3)+(4*7)+(3*9)+(2*1)+(1*3)=99
99 % 10 = 9
So 4379-13-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H15NO/c1-3-5(2)6(7)4-8/h5-6,8H,3-4,7H2,1-2H3

4379-13-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name L-ISOLEUCINOL HYDROCHLORIDE

1.2 Other means of identification

Product number -
Other names 2-amino-3-methylpentan-1-ol

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:4379-13-9 SDS

4379-13-9Relevant articles and documents

Asymmetric Synthesis Using Chirally Modified Borohydrides. Part 1. Enantioselective Reduction of Aromatic Ketones with the Reagent Prepared from Borane and (S)-Valinol

Itsuno, Shinichi,Hirao, Akira,Nakahama, Seiichi,Yamazaki, Noboru

, p. 1673 - 1676 (2007/10/02)

The asymmetric reduction of aromatic ketones with the reagents prepared from borane and chiral aminoalcohols was studied under various conditions.The ratio of borane to (S)-valinol was found to be optimum at 2-3:1, when up to 65-73percent selectivity was obtained in the reduction of n-propyl phenyl ketone.The amino-alkoxy-amine-boranes (2) and/or (3) were tentatively proposed as the reaction species responsible for asymmetric induction.

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