6400-14-2

Basic information

• Product Name: 2-CHLORO-M-PHENYLENEDIAMINE
• Synonyms: 2-CHLORO-M-PHENYLENEDIAMINE;2-Chlorobenzene-1,3-diamine;3-Amino-2-chloroaniline
• CAS NO: 6400-14-2
• Molecular Formula: C₆H₇ClN₂
• Molecular Weight: 142.59
• Mol File: 6400-14-2.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C(protect from light)
• CAS DataBase Reference: 2-CHLORO-M-PHENYLENEDIAMINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-CHLORO-M-PHENYLENEDIAMINE(6400-14-2)
• EPA Substance Registry System: 2-CHLORO-M-PHENYLENEDIAMINE(6400-14-2)

Safety Data

• Hazardous Substances Data: 6400-14-2(Hazardous Substances Data)

Usage

General Description

2-Chloro-m-phenylenediamine, also known as 2-CMPD, is a chemical compound used primarily as an intermediate in the production of dyes and pigments. It is a derivative of phenylenediamine and contains a chlorine atom attached to the meta position of the phenyl ring. 2-CMPD is commonly employed in hair dyes due to its ability to produce vibrant color and long-lasting results. However, it is important to note that 2-CMPD is classified as a skin and respiratory irritant and can cause allergic reactions in some individuals. Therefore, it should be handled with care and appropriate safety measures should be taken when working with this chemical.

Upstream product

• 88-73-3 2-Chloronitrobenzene 
• 606-21-3 1-chloro-2,6-dinitrobenzene 

Downstream Products

• 916052-00-1 1,1-dimethylethyl 4-{2-[(4-chloro-3-{[(5Z)-4-oxo-5-(6-quinolinylmethylidene)-4,5-dihydro-1,3-thiazol-2-yl]amino}phenyl)amino]-2-oxoethyl}-1-piperazinecarboxylate 
• 916051-58-6 2-[3,4-bis(methyloxy)phenyl]-N-(4-chloro-3-{[(5Z)-4-oxo-5-(6-quinolinylmethylidene)-4,5-dihydro-1,3-thiazol-2-yl]amino}phenyl)acetamide 
• 916051-87-1 N-(4-chloro-3-{[(5Z)-4-oxo-5-(6-quinolinylmethylidene)-4,5-dihydro-1,3-thiazol-2-yl]amino}phenyl)-2-(1-piperidinyl)acetamide 
• 916051-42-8 N-(4-chloro-3-{[(5Z)-4-oxo-5-(6-quinolinylmethylidene)-4,5-dihydro-1,3-thiazol-2-yl]amino}phenyl)-N'-(phenylmethyl)urea 
• 916051-72-4 N-(4-chloro-3-{[(5Z)-4-oxo-5-(6-quinolinylmethylidene)-4,5-dihydro-1,3-thiazol-2-yl]amino}phenyl)-1-phenylmethanesulfonamide 
• 916051-25-7 N-(4-chloro-3-{[(5Z)-4-oxo-5-(6-quinolinylmethylidene)-4,5-dihydro-1,3-thiazol-2-yl]amino}phenyl)-2-(2-thienyl)acetamide 
• 916052-96-5 N-(2-chloro-3-{[(5Z)-4-oxo-5-(6-quinoxalinylmethylidene)-4,5-dihydro-1,3-thiazol-2-yl]amino}phenyl)cyclobutanecarboxamide 
• 916051-41-7 N-(4-chloro-3-{[(5Z)-4-oxo-5-(6-quinolinylmethylidene)-4,5-dihydro-1,3-thiazol-2-yl]amino}phenyl)-2-cyclopropylacetamide 
• 916053-11-7 N-(2-chloro-3-{[(5Z)-4-oxo-5-(6-quinoxalinylmethylidene)-4,5-dihydro-1,3-thiazol-2-yl]amino}phenyl)benzamide 
• 916052-94-3 N-(2-chloro-3-{[(5Z)-4-oxo-5-(6-quinoxalinylmethylidene)-4,5-dihydro-1,3-thiazol-2-yl]amino}phenyl)cyclopropanecarboxamide 
• 916052-73-8 4-chloro-N-(2-methylpropyl)-3-{[(5Z)-4-oxo-5-(6-quinoxalinylmethylidene)-4,5-dihydro-1,3-thiazol-2-yl]amino}benzamide 
• 916052-87-4 N-(2-chloro-3-{[(5Z)-4-oxo-5-(6-quinoxalinylmethylidene)-4,5-dihydro-1,3-thiazol-2-yl]amino}phenyl)-2-methylpropanamide 
• 916051-23-5 N-(4-chloro-3-{[(5Z)-4-oxo-5-(6-quinolinylmethylidene)-4,5-dihydro-1,3-thiazol-2-yl]amino}phenyl)propanamide 
• 916053-09-3 N-(2-chloro-3-{[(5Z)-4-oxo-5-(6-quinoxalinylmethylidene)-4,5-dihydro-1,3-thiazol-2-yl]amino}phenyl)methanesulfonamide 

Relevant articles and documents

Iron PCP Pincer Complexes in Three Oxidation States: Reversible Ligand Protonation to Afford an Fe(0) Complex with an Agostic C-H Arene Bond

In the current investigation, the reaction of Fe2(CO)9 with the ligand precursor 2-chloro-N1,N3-bis(diisopropylphosphanyl)-N1,N3-diethylbenzene-1,3-diamine (P(C-Cl)PNEt-iPr) (1)

Method for preparing halogenated aniline from halogenated nitrobenzene through catalytic hydrogenation

The invention discloses a method for preparing halogenated aniline from halogenated nitrobenzene through catalytic hydrogenation. The method comprises the following steps: in a reaction kettle, performing liquid phase catalytic hydrogenation reaction to halogenated nitrobenzene under the action of a sulfur-doped carbon material loaded noble metal catalyst, to obtain halogenated aniline shown in the formula (II), wherein the loading quantity of noble metal in the sulfur-doped carbon material loaded noble metal catalyst is 0.1-5wt%. In the method, the catalyst has good stability, the hydrogenation halogen removal side effect can be effectively inhibited under the condition of having no added halogen removal inhibitor, and the product selectivity is high.

Derivatives of 4,6 dioxopyrido[3,2-g]quinoline 2,8 dicarboxylic acid

Novel chemical compounds of the formula: SPC1 Wherein R is selected from the group consisting of hydrogen, alkyl from one to three carbon atoms, inclusive, phenyl, alkali metal, or an amine cation; X and Y can be the same or different and are selected from the group consisting of hydrogen, alkyl of from one to six carbon atoms, inclusive, cycloalkyl of 5 or 6 carbon atoms, inclusive, phenyl, hydroxyl, alkoxy having from one to three carbon atoms, inclusive, halogen, trifluoromethyl, cyano, carboxyamide and O C-OQ, EQU1 where Q is selected from the group consisting of hydrogen, alkyl from one to three carbon atoms, inclusive, alkali metal, and an amine cation, with the proviso that where R is hydrogen, alkali metal or an amine cation, then Q is the same as R, and where R is phenyl or alkyl from one to three carbon atoms, then Q is phenyl or alkyl from one to three carbon atoms; and Z is selected from the group consisting of hydrogen, alkyl from one to three carbon atoms, inclusive, and phenyl. The compounds are formulated with pharmaceutical carriers for oral or parenteral administration, with insufflation being the preferred method. The compositions are useful in the prophylactic treatment of sensitized humans and mammals for allergy and all anaphylactic reactions of a reagin or non-reagin mediated nature.