40130-97-0

Basic information

• Product Name: 2-chloro-5-methyl-4-nitrophenol
• Synonyms: 2-chloro-5-methyl-4-nitrophenol
• CAS NO: 40130-97-0
• Molecular Formula: C₇H₆ClNO₃
• Molecular Weight: 187.58044
• EINECS: 254-802-2
• Mol File: 40130-97-0.mol
• Article Data: 6

Chemical Properties

• Melting Point: 143-144 °C(Solv: benzene (71-43-2))
• Boiling Point: 301.8 °C at 760 mmHg
• Flash Point: 136.3 °C
• Appearance: /
• Density: 1.466 g/cm³
• Vapor Pressure: 0.000575mmHg at 25°C
• Refractive Index: 1.61
• Storage Temp.: 2-8°C
• PKA: 5.70±0.24(Predicted)
• CAS DataBase Reference: 2-chloro-5-methyl-4-nitrophenol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-chloro-5-methyl-4-nitrophenol(40130-97-0)
• EPA Substance Registry System: 2-chloro-5-methyl-4-nitrophenol(40130-97-0)

Safety Data

• Hazardous Substances Data: 40130-97-0(Hazardous Substances Data)

Usage

General Description

2-chloro-5-methyl-4-nitrophenol, also known as CMNP, is a chemical compound that belongs to the phenol class of organic compounds. It is a yellow crystalline substance with a molecular formula of C7H6ClNO3. CMNP is widely used as a selective herbicide in the agricultural industry, particularly for controlling broadleaf weeds in various crops. It works by inhibiting the enzyme acetolactate synthase, which is essential for the growth and production of essential amino acids in plants. In addition to its herbicidal properties, CMNP is also used as an intermediate in the production of other chemical compounds. However, it is important to handle CMNP with care, as it is toxic to aquatic organisms and can cause skin and eye irritation in humans.

InChI:InChI=1/C7H6ClNO3/c1-4-2-7(10)5(8)3-6(4)9(11)12/h2-3,10H,1H3

Upstream product

• 2581-34-2 3-methyl-4-nitrophenol 
• 62509-09-5 2-chloro-5-methyl-4-nitroso-phenol 
• 7782-50-5 chlorine 
• 64-19-7 acetic acid 
• 866996-99-8 1-chloro-4-methyl-2,5-dinitro-benzene 
• 7664-41-7 ammonia 
• 615-74-7 2-chloro-5-methylphenol 

Downstream Products

• 1071622-21-3 4-amino-2-chloro-5-methylphenol 
• 62492-45-9 2-nitro-4-chloro-5-methoxymethylbenzene 
• 62492-46-0 5-chloro-4-methoxy-2-methylaniline 
• 623161-78-4 [3-(2-chloro-5-methyl-4-nitrophenoxy)propyl]trimethylsilane 
• 63762-74-3 N-[2-(6-chloro-5-methoxy-indol-3-yl)-ethyl]-acetamide 
• 63762-71-0 2-chloro-5-<(β-dimethylamino)-vinyl>-4-nitroanisole 
• 99474-19-8 2-(4-chloro-5-methoxy-2-nitrophenyl)-1-dimethylamino ethylene 
• 63762-73-2 (6-chloro-5-methoxy-indol-3-yl)-acetonitrile 
• 63762-72-1 6-chloro-5-methoxy-1H-indole 
• 205192-97-8 6-chloro-5-phenylindoline 
• 162100-81-4 2-chloro-5-methyl-4-nitrobenzaldehyde 
• 162100-80-3 4-chloro-2-nitro-5-vinyltoluene 
• 162100-82-5 2-chloro-5-methyl-4-nitro-benzoic acid 
• 162100-79-0 trifluoromethanesulfonic acid 2-chloro-5-methyl-4-nitrophenyl ester 

Relevant articles and documents

NOVEL COMPOUNDS AND PHARMACEUTICAL COMPOSITIONS THEREOF FOR THE TREATMENT OF FIBROSIS

The present invention discloses compounds according to Formula (I) Wherein R1, R2, L, A1, A2, A3, Cy and the subscript n are as defined herein. The present invention relates to antagonists compounds of sphingosine 1-phosphate (SIP) receptor, methods for their production, pharmaceutical compositions comprising the same, and methods of treatment using the same, for the prophylaxis and/or treatment of diseases involving fibrotic diseases, inflammatory diseases, respiratory diseases, autoimmune diseases, metabolic diseases, cardiovascular diseases, and/or proliferative diseases by administering the compound of the invention.

Melatonin derivatives - I - Synthesis of N-succinyl-6-chloro-5-methoxytryptamine

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Synthesis and evaluation of the antiovulatory activity of a variety of melatonin analogues

A series of melatonin analogues was synthesized and examined for ovulation-blocking activity. Deviation from the 5-methoxy group or substitution of the 1 position prevented activity. Activity was not particularly sensitive to minor variations in the N-acyl group nor was it significantly altered by methylation of position 2 or the α-methylene; however, a pronounced enhancement resulted from halogenation of the 6 position.