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88912-27-0

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88912-27-0 Usage

General Description

3-Chloroisonicotinic acid is a chemical compound with the molecular formula C6H4ClNO2. It is a derivative of isonicotinic acid, with a chlorine atom substituted at the 3-position of the pyridine ring. 3-Chloroisonicotinic acid is used as a building block in organic synthesis and has potential applications in the pharmaceutical industry. It is also considered a versatile ligand in coordination chemistry, forming complexes with metal ions that have catalytic and biological relevance. 3-Chloroisonicotinic acid is a white solid with a slightly acidic nature and its properties make it a valuable ingredient in the manufacturing of various products.

Check Digit Verification of cas no

The CAS Registry Mumber 88912-27-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,9,1 and 2 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 88912-27:
(7*8)+(6*8)+(5*9)+(4*1)+(3*2)+(2*2)+(1*7)=170
170 % 10 = 0
So 88912-27-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H4ClNO2/c7-5-3-8-2-1-4(5)6(9)10/h1-3H,(H,9,10)

88912-27-0 Well-known Company Product Price

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  • Aldrich

  • (633410)  3-Chloropyridine-4-carboxylicacid  97%

  • 88912-27-0

  • 633410-1G

  • 222.30CNY

  • Detail
  • Aldrich

  • (633410)  3-Chloropyridine-4-carboxylicacid  97%

  • 88912-27-0

  • 633410-5G

  • 769.86CNY

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88912-27-0SDS

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 3-Chloroisonicotinic Acid

1.2 Other means of identification

Product number -
Other names 3-chloropyridine-4-carboxylic 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:88912-27-0 SDS

88912-27-0Relevant articles and documents

Synthesis and biological evaluation of new cytotoxic indazolo[4,3-gh] isoquinolinone derivatives

Shahabi, Manochehr,Schirmer, Eva,Shanab, Karem,Leepasert, Theerachart,Ruzicka, Jana,Holzer, Wolfgang,Spreitzer, Helmut,Aicher, Babette,Schmidt, Peter,Blumenstein, Lars,Müller, Gilbert,Günther, Eckhard

, p. 1846 - 1852 (2013/04/10)

A series of indazolo[4,3-gh]isoquinolinones derivatives have been synthesized to decrease cardiotoxic side effects in comparison to Mitoxantrone. The antiproliferative effects of different side chains were investigated and tested on at least four different cell lines of cervix, ovarian, CNS, NSCLC (non-small-cell lung cancer) and colon carcinoma. In addition to antiproliferative activities, influence on cell cycle and intercalation behavior have been tested.

Directed lithiation of unprotected pyridinecarboxylic acids: Syntheses of halo derivatives

Lazaar, Jalal,Rebstock, Anne-Sophie,Mongin, Florence,Godard, Alain,Trécourt, Fran?ois,Marsais, Francis,Quéguiner, Guy

, p. 6723 - 6728 (2007/10/03)

Deprotonation of all isomeric lithium pyridinecarboxylates and subsequent trapping with hexachloroethane or iodine afforded straightforward access to chloro- and iodopyridinecarboxylic acids, respectively. Starting from lithium 5-bromonicotinate, the introduction of an iodine atom at C4 and further halogen migration allowed the potential of this method to be extended to the synthesis of more elaborate derivatives.

Synthesis of regioisomeric 6,9-(chlorofluoro)-substituted benzo[g]quinoline-5,10-diones, benzo[g]isoquinoline-5,10-diones and 6-chloro-9-fluorobenzo[g]quinoxaline-5,10-dione

Krapcho, A. Paul,Gallagher, Cynthia E.,Hammach, Abdelhakim,Ellis, Michael,Menta, Ernesto,Oliva, Ambrogio

, p. 27 - 32 (2007/10/03)

Treatment of difluoro or chloro fluoro-substituted benzyl bromides 5a-c with zinc dust in tetrahydrofuran leads to the corresponding benzylic zinc bromides 6a-c. These organometallics on treatment with chlorosubstituted heterocyclic esters 4A and 4B mediated by nickel catalysis undergo couplings to yield dihalobenzyl substituted heterocyclic esters 7Aa-c and 7Ba-c. Treatment of 4c with 6c under Pd catalysis leads to 7Cc. The acids 8, prepared by hydrolysis of these esters, with treatment of fuming sulfuric acid undergo cyclizations and oxidations to yield the desired regioisomeric dihalo-substituted heterocyclic quinones 2.

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