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24242-19-1

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24242-19-1 Usage

Chemical Properties

Off-white Cryst

Uses

5-Aminonicotinic acid is used in the synthesis of coordination polymers, bioluminescent reagents and biological active agents.

Definition

ChEBI: 5-aminonicotinic acid is an aminonicotinic acid in which the amino group is situated at position 5 of the pyridine ring. It has a role as a metabolite. It is an aromatic amine, an aminopyridine and an aminonicotinic acid. It is functionally related to a nicotinic acid.

Check Digit Verification of cas no

The CAS Registry Mumber 24242-19-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,2,4 and 2 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 24242-19:
(7*2)+(6*4)+(5*2)+(4*4)+(3*2)+(2*1)+(1*9)=81
81 % 10 = 1
So 24242-19-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H6N2O2/c7-5-1-4(6(9)10)2-8-3-5/h1-3H,7H2,(H,9,10)/p-1

24242-19-1 Well-known Company Product Price

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  • Aldrich

  • (672513)  5-Aminopyridine-3-carboxylicacid  97%

  • 24242-19-1

  • 672513-1G

  • 1,282.32CNY

  • Detail
  • Aldrich

  • (672513)  5-Aminopyridine-3-carboxylicacid  97%

  • 24242-19-1

  • 672513-5G

  • 5,380.83CNY

  • Detail

24242-19-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-aminopyridine-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names 3-pyridinecarboxylic acid,5-amino

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:24242-19-1 SDS

24242-19-1Relevant articles and documents

Efforts toward the synthesis of (+)-Lyconadin A

Karella, Satish,Raghavan, Sadagopan

, (2020/08/10)

Abstract: Synthetic efforts toward the synthesis of (+)-lyconadin A are described. B-Alkyl Suzuki coupling is utilized for combining 2-iodo cyclohexenone with the piperidine subunit. The piperidine subunit is derived from 5-bromo-3-nicotinic acid, and iod

AZOLECARBOXAMIDE HERBICIDES

-

Page 46, (2010/02/06)

Compounds of Formula (I), and their N-oxides and agriculturally suitable salts, are disclosed which are useful for controlling undesired vegetation, wherein J is (J-1), (J-2,(J-3), (J-4), (J-5), (J-6), (J-7), (J-8) and R1a, R1b, R1c, R2a, R2b, R3, R4, R05, T, U, W, Y and Z are as defined in the disclosure. Also disclosed are compositions containing the compounds of Formula (I) and a method for controlling undesired vegetation which involves contacting the vegetation or its environment with an effective amount of a compound of Formula (I). Also disclosed are mixtures and compositions comprising a herbicidally effective amount of a compound of Formula (Iz) wherein J, R1a, R1b, R1c, R2a, R2b, R3, R4, R05, T, U, W, Y and Z are as defined in the disclosure; and an effective amount of another herbicide or herbicide safener. Also disclosed is a method for selectively controlling undesired vegetation in a crop that involves contacting the locus of a crop with an effective amount of a compound of Formula (Iz) and a effective amount of a safener.

Stereoelectronic substituent effects in polyhydroxylated piperidines and hexahydropyridazines

Jensen, Henrik Helligso,Lyngbye, Laila,Jensen, Astrid,Bols, Mikael

, p. 1218 - 1226 (2007/10/03)

From the pKa values of the conjugate acids of a large series of hydroxylated piperidines and hexahydropyridazines, a consistent difference in basicity was found between stereo-isomers having an axial or equatorial hydroxyl (OH) group either β o

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