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2-Chloro-5-nitrotoluene

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  • CAS:13290-74-9
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2-Chloro-5-nitrotoluene Basic information
Product Name:2-Chloro-5-nitrotoluene
Synonyms:5-NITRO-2-CHLOROTOLUENE;4-CHLORO-3-METHYLNITROBENZENE;2-CHLORO-5-NITROTOLUENE;2-CHLORO-5-NITROMETHYLBENZENE;BENZENE, 2-CHLORO-1-METHYL-5-NITRO-;2-Chloro-5-nitrotolune;2-CHLORO-1-METHYL-5-NITROBENZENE;1-chloro-2-methyl-4-nitro-benzen
CAS:13290-74-9
MF:C7H6ClNO2
MW:171.58
EINECS:236-306-8
Product Categories:Aromatic Hydrocarbons (substituted) & Derivatives;Nitro Compounds;Nitrogen Compounds;Organic Building Blocks;Halogen toluene;Chlorine Compounds;Nitro Compounds
Mol File:13290-74-9.mol
2-Chloro-5-nitrotoluene Structure
2-Chloro-5-nitrotoluene Chemical Properties
Melting point 40-44 °C
Boiling point 94-96°C 4mm
density 1.3246 (rough estimate)
refractive index 1.5377 (estimate)
Fp 94-96°C/4mm
storage temp. Sealed in dry,Room Temperature
form powder to crystal
color White to Yellow to Green
BRN 2044766
InChI1S/C7H6ClNO2/c1-5-4-6(9(10)11)2-3-7(5)8/h2-4H,1H3
InChIKeyBGDCQZFFNFXYQC-UHFFFAOYSA-N
SMILESCc1cc(ccc1Cl)[N+]([O-])=O
CAS DataBase Reference13290-74-9(CAS DataBase Reference)
EPA Substance Registry System2-Chloro-5-nitrotoluene (13290-74-9)
Safety Information
Hazard Codes Xn,N
Risk Statements 22-52/53
Safety Statements 22-36/37-61
RIDADR UN 3457 6.1/PG 3
WGK Germany 3
TSCA TSCA listed
HazardClass 6.1
PackingGroup III
HS Code 2902900000
Storage Class6.1D - Non-combustible acute toxic Cat.3
toxic hazardous materials or hazardous materials causing chronic effects
Hazard ClassificationsAcute Tox. 4 Oral
MSDS Information
ProviderLanguage
2-Chloro-5-nitrotoluene English
SigmaAldrich English
ALFA English
2-Chloro-5-nitrotoluene Usage And Synthesis
Chemical Propertieswhite to light yellow crystal powder
Synthesis
2-Methyl-4-nitroaniline

99-52-5

2-Chloro-5-nitrotoluene

13290-74-9

General procedure for the synthesis of 2-chloro-5-nitrotoluene from 4-nitro-2-methylaniline: First, 152 kg of 2-amino-5-nitrotoluene was dissolved in 600 kg of concentrated sulfuric acid, followed by the addition of 150 kg of water, and naturally heated to 100°C. After the reaction solution was completely dissolved, the temperature was lowered to 300 kg of industrial hydrochloric acid at a concentration of 30%. After 2-amino-5-nitrotoluene was completely dissolved, the temperature was lowered and 300 kg of industrial hydrochloric acid with a mass concentration of 30% was added, during which it was necessary to ensure that the temperature of the reaction solution did not exceed 0°C. The temperature of the reaction solution was then increased by 27 kg at a constant rate. Next, 276 kg of a 25% sodium nitrite solution was added at a constant rate to produce the diazonium salt solution. In another reactor, 450 kg of industrial hydrochloric acid was added and 225 kg of cuprous chloride was dissolved with stirring, and the temperature was reduced to below 20°C after dissolution. The prepared diazonium salt solution was quickly added to this reactor for rapid stirring and hydrolysis reaction. The reaction mixture was held for 2 hours before being warmed up to 55°C and maintained at this temperature for 2 hours. Finally, water vapor was distilled out by increasing the temperature until 160 kg of 2-chloro-5-nitrotoluene was collected in 93.3% yield.

References[1] Patent: CN108373434, 2018, A. Location in patent: Paragraph 0032; 0033; 0035; 0036; 0037; 0040; 0041
[2] Chemische Berichte, 1887, vol. 20, p. 200
[3] Arzneimittel-Forschung/Drug Research, 1989, vol. 39, # 9, p. 1073 - 1080
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