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343781-57-7

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343781-57-7 Usage

General Description

2,5-Dichloro-4-hydroxypyridine is a chemical compound with the molecular formula C5H3Cl2NO. It is a chlorinated derivative of pyridine, containing two chlorine atoms and a hydroxyl group. 2,5-Dichloro-4-hydroxypyridine is commonly used in the synthesis of pharmaceuticals and agrochemicals due to its versatile reactivity and ability to form complex organic structures. It is a potent inhibitor of enzymes, making it useful in the development of new drug compounds. Additionally, its unique chemical properties make it valuable in the production of herbicides and pesticides. 2,5-Dichloro-4-hydroxypyridine is considered to be a hazardous chemical and should be handled and stored with caution to prevent any potential harm.

Check Digit Verification of cas no

The CAS Registry Mumber 343781-57-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,3,7,8 and 1 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 343781-57:
(8*3)+(7*4)+(6*3)+(5*7)+(4*8)+(3*1)+(2*5)+(1*7)=157
157 % 10 = 7
So 343781-57-7 is a valid CAS Registry Number.
InChI:InChI=1/C5H3Cl2NO/c6-3-2-8-5(7)1-4(3)9/h1-2H,(H,8,9)

343781-57-7SDS

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 2,5-DICHLORO-4-HYDROXYPYRIDINE

1.2 Other means of identification

Product number -
Other names 2,5-dichloropyridin-4-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:343781-57-7 SDS

343781-57-7Relevant articles and documents

Efficient synthesis of halohydroxypyridines by hydroxydeboronation

Voisin, Anne Sophie,Bouillon, Alexandre,Lancelot, Jean-Charles,Rault, Sylvain

, p. 1417 - 1421 (2007/10/03)

This paper describes a general method for the synthesis of halohydroxypyridines from novel halopyridinylboronic acids and esters recently described by some of us. Halopyridinylboronic acids and esters have been efficiently hydroxydeboronated under mild conditions by employing hydrogen peroxide or meta-chloroperbenzoic acid. These hydroxylations take place regioselectively without other oxidation (N-oxide formation).

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