36286-75-6

Basic information

• Product Name: 4-CHLORO-BENZENECARBOXIMIDIC ACID, HYDRAZIDE
• Synonyms: 4-CHLORO-BENZENECARBOXIMIDIC ACID, HYDRAZIDE
• CAS NO: 36286-75-6
• Molecular Formula: C₇H₈ClN₃
• Molecular Weight: 169.61
• Mol File: 36286-75-6.mol
• Article Data: 2

Chemical Properties

• Melting Point: 89-92 °C
• Boiling Point: 318.7 °C at 760 mmHg
• Flash Point: 146.6 °C
• Appearance: /
• Density: 1.36 g/cm³
• Vapor Pressure: 0.000354mmHg at 25°C
• Refractive Index: 1.622
• PKA: 8.09±0.50(Predicted)
• CAS DataBase Reference: 4-CHLORO-BENZENECARBOXIMIDIC ACID, HYDRAZIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-CHLORO-BENZENECARBOXIMIDIC ACID, HYDRAZIDE(36286-75-6)
• EPA Substance Registry System: 4-CHLORO-BENZENECARBOXIMIDIC ACID, HYDRAZIDE(36286-75-6)

Safety Data

• Hazardous Substances Data: 36286-75-6(Hazardous Substances Data)

Usage

General Description

4-CHLORO-BENZENECARBOXIMIDIC ACID, HYDRAZIDE is a chemical compound with the molecular formula C7H7ClN2O. It is commonly used as a pesticide and herbicide, particularly in the control of weeds in agricultural settings. 4-CHLORO-BENZENECARBOXIMIDIC ACID, HYDRAZIDE is also used in the production of pharmaceuticals and other organic compounds. It is classified as a hazardous substance and should be handled with caution due to its potential for causing skin and eye irritation, as well as respiratory issues if inhaled. Additionally, it has been reported to have harmful effects on aquatic life and the environment, so it should be used and disposed of properly to minimize its impact.

InChI:InChI=1/C7H8ClN3/c8-6-3-1-5(2-4-6)7(9)11-10/h1-4H,10H2,(H2,9,11)

Upstream product

• 623-03-0 4-Cyanochlorobenzene 
• 64-17-5 ethanol 

Downstream Products

• 89730-55-2 6-Amino-3-(4-chlorphenyl)-1,2,4-triazin-5(2H)-on 
• 126542-16-3 3-(4-Chloro-phenyl)-5-oxo-2,5-dihydro-[1,2,4]triazine-6-carboxylic acid methyl ester 
• 81945-81-5 7-(4-Chloro-phenyl)-2,3a,5-triphenyl-3,3a-dihydro-pyrazolo[1,5-c]pyrimidine 
• 109948-30-3 3-(4-Chloro-phenyl)-5-[(2-oxo-1,2-diphenyl-ethyl)-phenyl-amino]-1H-[1,2,4]triazin-6-one 
• 87522-18-7 2-p-chlorophenyl-4-oxido-6,8-diphenylpyrido<2,1-f><1,2,4>triazin-9-ium 
• 126542-15-2 3-(4-Chloro-phenyl)-6-phenyl-2H-[1,2,4]triazin-5-one 
• 36286-77-8 ethyl 3-(4-chlorophenyl)-5-oxo-4,5-dihydro-1,2,4-triazine-6-carboxylate 
• 1003046-47-6 3-(p-chlorophenyl)phenanthro[9,10-e][1,2,4]triazine 
• 126542-35-6 ethyl 5-chloro-3-(4-chlorophenyl)-1,2,4-triazine-6-carboxylate 
• 89730-63-2 6-Amino-3-(4-chlorphenyl)-1,2,4-triazin-5(2H)-thion 
• 126542-25-4 5-Chloro-3-(4-chloro-phenyl)-6-phenyl-[1,2,4]triazine 
• 126542-26-5 5-Chloro-3-(4-chloro-phenyl)-[1,2,4]triazine-6-carboxylic acid methyl ester 
• 126542-77-6 5-But-3-ynyloxy-3-(4-chloro-phenyl)-6-phenyl-[1,2,4]triazine 
• 62230-37-9 3-(4-chlorophenyl)-5-phenyl-1,2,4-triazine 

Relevant articles and documents

Novel 6-azapteridines from bifunctional 1,2,4-triazines

The convergent synthesis of ethyl 5-chloro- and 5-amino-3-aryl-1,2,4-triazinecarboxylates 9a-9d and 10a-10d as well as of 5-amino-3-aryl-1,2,4-triazine-6-carboxamides 11a-11d is described. Compounds 9, 10 and 11 are powerful key compounds for cyclization reactions to the novel pyrimido[4,5-e][1,2,4]triazines 13d, 14c, 14d, 15c and 17a, 17d.