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89836-93-1

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89836-93-1 Usage

Uses

L-Leucine-2-d1 (CAS# 89836-93-1) is a useful isotopically labeled research compound.

Check Digit Verification of cas no

The CAS Registry Mumber 89836-93-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,8,3 and 6 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 89836-93:
(7*8)+(6*9)+(5*8)+(4*3)+(3*6)+(2*9)+(1*3)=201
201 % 10 = 1
So 89836-93-1 is a valid CAS Registry Number.

89836-93-1SDS

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 L-LEUCINE-2-D1

1.2 Other means of identification

Product number -
Other names homoserine lactone*HBr

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:89836-93-1 SDS

89836-93-1Downstream Products

89836-93-1Relevant articles and documents

Deuterated pyrrolidone derivative Pharmaceutical compositions and uses thereof

-

Paragraph 0077-0079, (2021/10/27)

The invention relates to a deuterated pyrrolidone derivative and a preparation method thereof, and also relates to application of the deuterated pyrrolidone derivative and a pharmaceutical composition thereof in treatment and prevention of metabolic disorder related diseases, and belongs to the field of medicines.

Development and Scale-Up of Stereoretentive α-Deuteration of Amines

Michelotti, Alessia,Rodrigues, Fabien,Roche, Maxime

supporting information, p. 1741 - 1744 (2017/11/24)

A stereoretentive deuteration of amino acids and amines has been developed using ruthenium on carbon catalyst, hydrogen gas at atmospheric pressure, and deuterium oxide as a source of deuterium. The process was successfully scaled-up, avoiding the use of expensive and sensitive catalyst and avoiding the use of deuterium gas under pressure. High deuterium incorporation and high yield of labeled compounds were obtained by a simple filtration process.

Enantioselective synthesis of α-deuterium labelled chiral α-amino acids via dynamic kinetic resolution of racemic azlactones

Oh, Joong-Suk,Kim, Kyung Il,Song, Choong Eui

supporting information; experimental part, p. 7983 - 7985 (2012/01/04)

Catalytic dynamic kinetic resolution (DKR) of racemic azlactones with EtOD using squaramide-based dimeric cinchona alkaloid organocatalysts is shown to be a highly effective strategy for the preparation of enantiomerically pure α-deuterated chiral α-amino

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