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4-AMINO-3-CHLORO-PYRIDINE-2-CARBOXYLIC ACID is a heterocyclic chemical compound characterized by a pyridine ring with an amino group at the 4 position, a chlorine atom at the 3 position, and a carboxylic acid group at the 2 position. 4-AMINO-3-CHLORO-PYRIDINE-2-CARBOXYLIC ACID is known for its potential pharmaceutical applications, primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. The versatile reactivity of 4-AMINO-3-CHLORO-PYRIDINE-2-CARBOXYLIC ACID, coupled with its ability to act as a building block for more complex molecules, positions it as a promising candidate in the development of new drugs and agrochemicals.

76165-18-9

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76165-18-9 Usage

Uses

Used in Pharmaceutical Industry:
4-AMINO-3-CHLORO-PYRIDINE-2-CARBOXYLIC ACID is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to form amide, ester, and peptide derivatives. Its presence in the molecular structure of drugs can contribute to their therapeutic effects and pharmacological properties.
Used in Agrochemical Industry:
In the agrochemical sector, 4-AMINO-3-CHLORO-PYRIDINE-2-CARBOXYLIC ACID serves as an intermediate in the development of agrochemicals, potentially enhancing the effectiveness of pesticides, herbicides, and other agricultural chemicals. Its reactivity allows for the creation of new molecules with targeted actions against pests or weeds.
Used in Research and Development:
4-AMINO-3-CHLORO-PYRIDINE-2-CARBOXYLIC ACID is utilized in research laboratories for the exploration of new chemical reactions and the synthesis of novel compounds. Its unique structure and functional groups make it an interesting subject for scientific inquiry and potential innovation in chemical and medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 76165-18-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,1,6 and 5 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 76165-18:
(7*7)+(6*6)+(5*1)+(4*6)+(3*5)+(2*1)+(1*8)=139
139 % 10 = 9
So 76165-18-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H5ClN2O2/c7-4-3(8)1-2-9-5(4)6(10)11/h1-2H,(H2,8,9)(H,10,11)

76165-18-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-amino-3-chloropyridine-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 4-Amino-3-Chloro-2-Pyridinecarboxylic 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:76165-18-9 SDS

76165-18-9Upstream product

76165-18-9Downstream Products

76165-18-9Relevant academic research and scientific papers

Degradation of benomyl, picloram, and dicamba in a conical apparatus by zero-valent iron powder

Ghauch, Antoine

, p. 1109 - 1117 (2001)

Reduction of some pesticides (benomyl, picloram, and dicamba) was studied in an aerobic batch conical pilot system to investigate the disappearance of these pesticides on contact with iron powder (20 g/l, 325-mesh). Aqueous buffered solutions of the compounds were added to the system followed by zero-valent iron powder (ZVIP), and the decline in the pesticide concentrations was monitored over time. HPLC analyses show a complete disappearance of picloram (1.20 mg/l) after 20 min of reaction. Benomyl (1.00 mg/l) and dicamba (1.25 mg/l) disappear after 25 and 40 min, respectively. The t50 values ranged from 3 to 5.5 min, and were about slightly less than the t1/2 values reported when the log of the relative HPLC peak area was plotted versus time, where the relative peak area was calculated by dividing the measured peak area by the initial peak area. Pathways for the degradation of the studied pesticides by ZVIP are proposed.

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