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56187-37-2

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56187-37-2 Usage

Chemical Properties

white powder

Uses

3,5-Dichloro-4-pyridone-1-acetic acid is used as an organic chemical synthesis intermediate.

Check Digit Verification of cas no

The CAS Registry Mumber 56187-37-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,1,8 and 7 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 56187-37:
(7*5)+(6*6)+(5*1)+(4*8)+(3*7)+(2*3)+(1*7)=142
142 % 10 = 2
So 56187-37-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H5Cl2NO3/c8-4-1-10(3-6(11)12)2-5(9)7(4)13/h1-2H,3H2,(H,11,12)/p-1

56187-37-2 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (B25471)  3,5-Dichloro-4-pyridone-1-acetic acid, 98%   

  • 56187-37-2

  • 5g

  • 719.0CNY

  • Detail
  • Alfa Aesar

  • (B25471)  3,5-Dichloro-4-pyridone-1-acetic acid, 98%   

  • 56187-37-2

  • 25g

  • 2979.0CNY

  • Detail

56187-37-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-Dichloro-4-pyridone-N-acetic acid

1.2 Other means of identification

Product number -
Other names 2-(3,5-dichloro-4-oxopyridin-1-yl)acetic acid

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:56187-37-2 SDS

56187-37-2Relevant articles and documents

Preparation method of 3,5-dihalogenated-4-pyridone-1-acetic acid

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Paragraph 0056-0057, (2019/12/02)

The invention provides a preparation method of 3, 5-dihalogenated-4-pyridone-1-acetic acid, and particularly relates to a preparation method of 3,5-dichloro-4-pyridone-1-acetic acid. The method comprises the following steps: performing a substitution reaction on piperidine-4-ketone hydrochloride (II) with chloroacetic acid in the presence of a proper solvent and an acid-binding agent to obtain 4-piperidone-1-acetic acid (III), carrying out a halogenation reaction on the 4-piperidone-1-acetic acid (III) and a halogenation reagent to obtain 3,3,5,5-tetrahalogenated-4-piperidone-1-acetic acid (IV), carrying out an elimination reaction in the presence of an alkali to remove hydrogen halide, and performing acidification with hydrochloric acid to obtain the 3,5-dihalo-4-pyridinone-1-acetic acid.The method has the advantages of cheap and easily available raw materials, low cost, simple operation, easy realization, less wastewater generation amount, environmental protection, high reaction selectivity, high product yield and purity, and suitableness for industrial production.

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