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41013-47-2

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41013-47-2 Usage

Description

(2S,3S)-(-)-2,3-Butanediamine dihydrochloride is a chiral chemical compound derived from 2,3-butanediamine, featuring two amino groups. The dihydrochloride form signifies its combination with two molecules of hydrochloric acid. (2S,3S)-(-)-2,3-BUTANEDIAMINE DIHYDROCHLORIDE is a crucial building block in the synthesis of pharmaceuticals, agrochemicals, and organic compounds, and is also utilized as a chiral resolving agent in chiral chromatography and as a chiral auxiliary in asymmetric synthesis. The (2S,3S) enantiomer configuration is vital for producing enantiomerically pure molecules, providing specific chiral properties to the final products.

Uses

Used in Pharmaceutical Industry:
(2S,3S)-(-)-2,3-BUTANEDIAMINE DIHYDROCHLORIDE is used as a building block for the synthesis of various pharmaceuticals, contributing to the development of new drugs and medicines.
Used in Agrochemical Industry:
(2S,3S)-(-)-2,3-BUTANEDIAMINE DIHYDROCHLORIDE is used as a building block for the synthesis of agrochemicals, aiding in the creation of effective and targeted agricultural products.
Used in Organic Synthesis:
(2S,3S)-(-)-2,3-BUTANEDIAMINE DIHYDROCHLORIDE is used as a building block in organic synthesis, enabling the production of a wide range of organic compounds.
Used in Chiral Chromatography:
(2S,3S)-(-)-2,3-BUTANEDIAMINE DIHYDROCHLORIDE is used as a chiral resolving agent, facilitating the separation and analysis of enantiomers in chiral chromatography.
Used in Asymmetric Synthesis:
(2S,3S)-(-)-2,3-BUTANEDIAMINE DIHYDROCHLORIDE is used as a chiral auxiliary in asymmetric synthesis, helping to produce enantiomerically pure molecules with specific chiral properties.

Check Digit Verification of cas no

The CAS Registry Mumber 41013-47-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,0,1 and 3 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 41013-47:
(7*4)+(6*1)+(5*0)+(4*1)+(3*3)+(2*4)+(1*7)=62
62 % 10 = 2
So 41013-47-2 is a valid CAS Registry Number.

41013-47-2SDS

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 (2S,3S)-(-)-2,3-BUTANEDIAMINE DIHYDROCHLORIDE

1.2 Other means of identification

Product number -
Other names L-threo-2.3-diamino-butane,dihydrochloride

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:41013-47-2 SDS

41013-47-2Upstream product

41013-47-2Downstream Products

41013-47-2Relevant articles and documents

De novo synthesis of tamiflu via a catalytic asymmetric ring-opening of meso-aziridines with TMSN3

Fukuta, Yuhei,Mita, Tsuyoshi,Fukuda, Nobuhisa,Kanai, Motomu,Shibasaki, Masakatsu

, p. 6312 - 6313 (2007/10/03)

An asymmetric ring-opening reaction of meso-aziridines with TMSN3 was developed using a catalyst prepared from Y(OiPr)3 and chiral ligand 2 in a 1:2 ratio. Excellent enantioselectivity was realized from a wide range of substrates with a practical catalyst loading. The products were efficiently converted to enantiomerically enriched 1,2-diamines, which are versatile chiral building blocks for pharmaceuticals and chiral ligands. This reaction was applied to a catalytic asymmetric synthesis of Tamiflu, a very important anti-influenza drug containing a chiral 1,2-diamino functionality. Copyright

Electrochemical reduction of ketoximes of some cycloalkanones and 1,2-diones

Prasad,Yadava,Mishra,Misra

, p. 95 - 97 (2007/10/02)

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