88-86-8

Basic information

• Product Name: 2,5-Dichloro-3-nitrobenzoic acid
• Synonyms: 2,5-dichloro-3-nitrobenzoic;TIMTEC-BB SBB003246;2,5-DICHLORO-3-NITROBENZOIC ACID;DINOBEN;DINOBEN:2,5-DICHLORO-3-NITROBENZOIC ACID;3-nitro-2,5-dichlorobenzoic acid;2,5-Dichloro-3-nitrobenzoic acid, 98+%;2,5-Dichloro-3-nitro
• CAS NO: 88-86-8
• Molecular Formula: C₇H₃Cl₂NO₄
• Molecular Weight: 236.01
• EINECS: 201-862-2
• Product Categories: Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts;Benzoic acid;C7;Carbonyl Compounds;Carboxylic Acids
• Mol File: 88-86-8.mol
• Article Data: 6

Chemical Properties

• Melting Point: 216-220 °C(lit.)
• Boiling Point: 366.5 °C at 760 mmHg
• Flash Point: 175.5 °C
• Appearance: /
• Density: 1.713 g/cm³
• Vapor Pressure: 5.11E-06mmHg at 25°C
• Refractive Index: 1.638
• Storage Temp.: Sealed in dry,Room Temperature
• PKA: 1.56±0.20(Predicted)
• BRN: 1976119
• CAS DataBase Reference: 2,5-Dichloro-3-nitrobenzoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2,5-Dichloro-3-nitrobenzoic acid(88-86-8)
• EPA Substance Registry System: 2,5-Dichloro-3-nitrobenzoic acid(88-86-8)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36
• WGK Germany: 2
• RTECS: DG7875000
• HazardClass: IRRITANT
• Hazardous Substances Data: 88-86-8(Hazardous Substances Data)

Usage

Uses

2,5-Dichloro-3-nitrobenzoic Acid is used in process for the preparation of organic halides.

General Description

Effect of 2,5-dichloro-3-nitrobenzoic acid on growth and on polar auxin transport has been studied.

InChI:InChI=1/C7H3Cl2NO4/c8-3-1-4(7(11)12)6(9)5(2-3)10(13)14/h1-2H,(H,11,12)

Upstream product

• 355133-69-6 2,5-dichloro-3-nitrobenzaldehyde 
• 50-79-3 2,5-dichlorobenzoic acid 
• 77350-06-2 2,5-dichloro-3-nitro-terephthalic acid 
• 6361-23-5 2,5-dichloro-benzaldehyde 

Downstream Products

• 6324-51-2 2-amino-5-chloro-3-nitrobenzoic acid 
• 1055331-49-1 (5-chloro-2-(4-fluoro-2-(hydroxymethyl)phenylthio)-3-nitrophenyl)methanol 
• 1055331-51-5 (2-chloro-8-fluorodibenzo[b,d]thiophene-4,6-diyl)dimethanol 
• 1055331-50-4 (2-(2-amino-4-chloro-6-(hydroxymethyl)phenylthio)-5-fluorophenyl)methanol 
• 1403595-49-2 C₁₃H₁₅Cl₂NO₂ 
• 1403595-48-1 methyl 2,5-dichloro-3-(cyclopentyl(methyl)amino)benzoate 
• 34408-25-8 methyl 2,5-dichloro-3-nitrobenzoate 
• 219963-62-9 2-chloro-3-bromo-5-chloronitrobenzene 
• 1055331-48-0 2-(2-carboxy-4-fluorophenylthio)-5-chloro-3-nitrobenzoic acid 
• 7286-84-2 methyl 2,5-dichloro-3-aminobenzoate 
• 355133-69-6 2,5-dichloro-3-nitrobenzaldehyde 
• 137332-57-1 (+)-(S)-N-(2,5-Dichloro-3-nitrobenzyl)-1,2-propanediamine 

Relevant articles and documents

SUBSTITUTED BENZENE COMPOUNDS

The present invention relates to substituted benzene compounds. The present invention also relates to pharmaceutical compositions containing these compounds and methods of treating cancer by administering these compounds and pharmaceutical compositions to subjects in need thereof. The present invention also relates to the use of such compounds for research or other non-therapeutic purposes.

INHIBITORS OF STEAROYL-COA DESATURASE

Provided herein are compounds of the formula (I): as well as pharmaceutically acceptable salts thereof, wherein the substituents are as those disclosed in the specification. These compounds, and the pharmaceutical compositions containing them, are useful for the treatment of diseases such as, for example, obesity.

Terephthalic acid derivatives

The novel compounds of the formula: STR1 wherein R1 and R2 are each either hydrogen or an alkyl group containing from 1 to 4 carbon atoms, and maybe the same or different, are useful intermediates in a novel process for the preparation of herbicidally active compounds such as 2,5-dichloro-3-nitro-benzoic acid, 2,5-dichloro-3-amino-benzoic acid and their functional derivatives.