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15410-44-3

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15410-44-3 Usage

General Description

2,3-Butanediol,1,4-dibromo-, (2R,3R)- is a chemical compound with the molecular formula C4H8Br2O2. It is a derivative of butanediol, containing bromine atoms at positions 1 and 4 on the molecule. The (2R,3R) designation indicates the stereochemistry of the compound, with the bromine atoms oriented in a specific configuration. This chemical is often used in organic synthesis and as a reagent in various reactions. It may also have applications in pharmaceuticals and other industries due to its unique structure and properties.

Check Digit Verification of cas no

The CAS Registry Mumber 15410-44-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,4,1 and 0 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 15410-44:
(7*1)+(6*5)+(5*4)+(4*1)+(3*0)+(2*4)+(1*4)=73
73 % 10 = 3
So 15410-44-3 is a valid CAS Registry Number.

15410-44-3SDS

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 2,3-Butanediol,1,4-dibromo-, (2R,3R)-

1.2 Other means of identification

Product number -
Other names 1,4-dibromo-L-1,4-dideoxy-threitol

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:15410-44-3 SDS

15410-44-3Relevant articles and documents

Kinetic resolution of d,l-1,2-diols catalyzed by amine-phosphinite bifunctional organocatalysis derived from quinidine

Mizuta, Shinya,Ohtsubo, Yutaka,Tsuzuki, Takeo,Fujimoto, Tetsuya,Yamamoto, Iwao

, p. 8227 - 8229 (2007/10/03)

Racemic C2-symmetric 1,2-diols were kinetically resolved by the acylation reaction catalyzed by the phosphinite derivative of quinidine to afford the corresponding monoacylated product with good to high enantioselectivities.

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