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3-chloro-2-hydroxybutanenitrile is an organic compound with the chemical formula C4H6ClNO. It is a colorless liquid with a molecular weight of 121.55 g/mol. 3-chloro-2-hydroxybutanenitrile is characterized by the presence of a chloro group (-Cl) at the third carbon, a hydroxyl group (-OH) at the second carbon, and a nitrile group (-CN) at the end of the four-carbon chain. It is synthesized through various chemical reactions and is used in the production of pharmaceuticals, agrochemicals, and other industrial applications. Due to its reactivity and potential toxicity, it is important to handle 3-chloro-2-hydroxybutanenitrile with proper safety measures and in accordance with relevant regulations.

5347-54-6

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5347-54-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5347-54-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,4 and 7 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5347-54:
(6*5)+(5*3)+(4*4)+(3*7)+(2*5)+(1*4)=96
96 % 10 = 6
So 5347-54-6 is a valid CAS Registry Number.

5347-54-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-chloro-2-hydroxybutanenitrile

1.2 Other means of identification

Product number -
Other names -

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:5347-54-6 SDS

5347-54-6Upstream product

5347-54-6Downstream Products

5347-54-6Relevant academic research and scientific papers

Method for preparing L-carnitine

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, (2008/06/13)

L-carnitine is prepared by a synthesizing process starting from D-mannitol. The synthesis is started with the formation of a D-mannitol ketonide (more specifically D-mannitol acetonide from D-mannitol and acetone, whereafter the D-mannitol is split by oxidation to give glyceraldehyde acetonide, which is further reduced to glycerol acetonide. Then the free hydroxyl group is exchanged with a halogen atom (chlorine) with the formation of chlorodihydroxy propane, the primary alcoholic group of which is functionalized with the acid chloride of a sulfonic acid (tosylchloride). The reaction of the tosyl derivative with the salt of hydrogen cyanide leads to the formation of the corresponding nitrile which, when reacted with trimethylamine gives carnitinonitrile. The nitrile group is now hydrolyzed to give L-carnitine chloride. The formation of L-carnitine can then be obtained by exchanging the chloride ion with a hydroxyl ion.

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