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16179-97-8

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16179-97-8 Usage

Description

2-Pyridylacetic acid hydrochloride is an organic compound that serves as a crucial intermediate in various chemical syntheses. It is characterized by its white to off-white solid appearance and is known for its role in the production of pharmaceuticals, agrochemicals, and dyestuff.

Uses

Used in Organic Synthesis:
2-Pyridylacetic acid hydrochloride is used as an important raw material and intermediate in the field of organic synthesis. Its unique chemical structure allows it to be a versatile building block for the creation of a wide range of compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-Pyridylacetic acid hydrochloride is utilized as an intermediate for the development of various drugs. Its properties make it suitable for the synthesis of medicinal compounds with potential therapeutic applications.
Used in Agrochemicals:
2-Pyridylacetic acid hydrochloride is also employed in the agrochemical industry, where it is used as a key component in the synthesis of pesticides and other agricultural chemicals.
Used in Dye Industry:
The dye industry benefits from the use of 2-Pyridylacetic acid hydrochloride as an intermediate in the production of various dyes, thanks to its ability to contribute to the formation of diverse colorants.
Used in Nucleophilic Substitution:
2-Pyridylacetic acid hydrochloride is utilized in nucleophilic substitution reactions, a fundamental class of chemical reactions in organic chemistry. Its participation in these reactions allows for the creation of new compounds with different functional groups, expanding the range of possible applications.

Check Digit Verification of cas no

The CAS Registry Mumber 16179-97-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,1,7 and 9 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 16179-97:
(7*1)+(6*6)+(5*1)+(4*7)+(3*9)+(2*9)+(1*7)=128
128 % 10 = 8
So 16179-97-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H7NO2/c9-7(10)5-6-3-1-2-4-8-6/h1-4H,5H2,(H,9,10)/p-1

16179-97-8 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
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  • Alfa Aesar

  • (L04870)  2-Pyridineacetic acid hydrochloride, 99%   

  • 16179-97-8

  • 5g

  • 353.0CNY

  • Detail
  • Alfa Aesar

  • (L04870)  2-Pyridineacetic acid hydrochloride, 99%   

  • 16179-97-8

  • 25g

  • 1408.0CNY

  • Detail
  • Aldrich

  • (P65606)  2-Pyridylaceticacidhydrochloride  99%

  • 16179-97-8

  • P65606-5G

  • 349.83CNY

  • Detail
  • Aldrich

  • (P65606)  2-Pyridylaceticacidhydrochloride  99%

  • 16179-97-8

  • P65606-25G

  • 1,374.75CNY

  • Detail

16179-97-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Pyridylacetic acid hydrochloride

1.2 Other means of identification

Product number -
Other names pyrid-2-ylacetic acid hydrochloride

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:16179-97-8 SDS

16179-97-8Upstream product

16179-97-8Relevant articles and documents

Oxidative decarbonylation of β-arylpyruvic acids using sodium perborate

Morrow, Nicholas,Ramsden, Christopher A.,Sargent, Bruce J.,Wallett, Christiaan D.

, p. 9603 - 9612 (1998)

Oxidation of β-aryl- and β-heteroarylpyruvic acids using sodium perborate tetrahydrate (SPB) in aqueous solution at ambient temperature gives the corresponding arylacetic acids in good yield (68-86%). The mild conditions are convenient for the preparation of thermally unstable acids. In particular the method has been applied to the preparation of an unstable 5- nitroimidazol-2-yl ethanoic acid which could not be obtained using other reagents apparently due to enolisation of the pyruvic acid precursor. Attempts to achieve decarbonylation using calcium hypochlorite or SPB in acidic solution lead to the 2 chloromethyl derivatives. The novel 5- nitroimidazol-2-yl ethanoic acid, which was required as a precursor of molecules of biological interest, has been fully characterised and converted to a known amide. Reaction of this acid with Vilsmeier's reagent gave an enamine derivative and not the expected vinamidinium salt. This novel mode of reaction is attributable to intramolecular hydrogen-bonding and favourable conjugation.

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