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2-Chloro-5-nitrobenzotrifluoride

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CAS:777-37-7
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CAS:777-37-7
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CAS:777-37-7
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2-Chloro-5-nitrobenzotrifluoride manufacturers

2-Chloro-5-nitrobenzotrifluoride Basic information
Product Name:2-Chloro-5-nitrobenzotrifluoride
Synonyms:2-Chloro-5-nitrobenzotrifluoride 98%;2-Chloro-5-nitrobenzotrifluoride98%;2-chloro-5-nitro trifluoromethylbenzene;2-chloro-5-nitrobenzotrifuoride;Nitro-2-(trifluoromethyl)chlorobenzene;2-Chloro-5-nitro-1-trifluoromethylbenzene;1-Chloro-2-(trifluoromethyl)-4-nitrobenzene;1-Chloro-4-nitro-6-trifluoromethylbenzene
CAS:777-37-7
MF:C7H3ClF3NO2
MW:225.55
EINECS:212-287-1
Product Categories:Trifluoromethylbenzene serise;API Intermediate;alkyl chloride| nitro-compound
Mol File:777-37-7.mol
2-Chloro-5-nitrobenzotrifluoride Structure
2-Chloro-5-nitrobenzotrifluoride Chemical Properties
Melting point 22°C
Boiling point 108 °C/10 mmHg (lit.)
density 1.527 g/mL at 25 °C (lit.)
refractive index n20/D 1.508(lit.)
Fp 210 °F
storage temp. Sealed in dry,Room Temperature
form powder to lump to clear liquid
Specific Gravity1.527
color White or Colorless to Yellow
FreezingPoint 20.0 to 23.0 ℃
BRN 2216169
Exposure limitsACGIH: TWA 2.5 mg/m3
NIOSH: IDLH 250 mg/m3
InChI1S/C7H3ClF3NO2/c8-6-2-1-4(12(13)14)3-5(6)7(9,10)11/h1-3H
InChIKeyHQROXDLWVGFPDE-UHFFFAOYSA-N
SMILES[O-][N+](=O)c1ccc(Cl)c(c1)C(F)(F)F
CAS DataBase Reference777-37-7(CAS DataBase Reference)
NIST Chemistry ReferenceBenzene, 1-chloro-4-nitro-2-(trifluoromethyl)-(777-37-7)
EPA Substance Registry System2-Chloro-5-nitrobenzotrifluoride (777-37-7)
Safety Information
Hazard Codes Xn,Xi
Risk Statements 22-36/37/38-20/21/22
Safety Statements 26-36/37/39-36
RIDADR 2810
WGK Germany 3
Hazard Note Irritant
TSCA TSCA listed
HazardClass 6.1
PackingGroup III
HS Code 29039990
Storage Class10 - Combustible liquids
Hazard ClassificationsAcute Tox. 4 Oral
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
MSDS Information
ProviderLanguage
4-Nitro-2-(trifluoromethyl)chlorobenzene English
ACROS English
SigmaAldrich English
ALFA English
2-Chloro-5-nitrobenzotrifluoride Usage And Synthesis
Chemical PropertiesClear colourless to light yellow liquid
Uses2-Chloro-5-nitrobenzotrifluoride is a polysubstituted organic fluorotoluene analogue. Its molecular structure has a reactive group chlorine atom at the 2-position and a nitro group at the 5-position. Therefore, the substance has high chemical reactivity and is widely used in the field of organic synthesis. It can be used to prepare asymmetric and symmetric diamine monomers containing trifluoromethyl groups, which in turn can be used to further prepare soluble polyimide, a multifunctional molecular material[1].
Synthesis
2-Chlorobenzotrifluoride

88-16-4

2-Chloro-5-nitrobenzotrifluoride

777-37-7

1) 400 g of o-chlorobenzotrifluoride (Feedstock I) was added to Preheating Module 2. Concentrated sulfuric acid (Feedstock II) and concentrated nitric acid (Feedstock III) were added to Preheating Module 1 for mixing and preheating, respectively. Subsequently, feedstocks I, II and III were introduced into the reaction module set for nitrification reaction. The flow rate of feedstock I was controlled to be 15 mL/min, the flow rate of feedstock II to be 18 mL/min, and the flow rate of feedstock III to be 11.5 mL/min by adjusting the flow pump. the reaction temperature was maintained at 60°C. The reaction temperature was maintained at 60°C. The flow rate of feedstock I was controlled to be 15 mL/min. The molar ratio of o-chlorobenzotrifluoride to nitric acid was 1:1.2, and the mass ratio of concentrated nitric acid to concentrated sulfuric acid was 1:4.0, and the reaction residence time was 55 seconds. The temperature of the cooling module was set to 25°C. The reaction solution at the outlet of the cooling module was collected for liquid-liquid separation. The product was combined with the organic phase by adding 270 mL of dichloromethane to the acid phase. It was washed with saturated sodium bicarbonate solution to neutrality and subsequently dried with anhydrous sodium sulfate. After evaporation of the solvent under reduced pressure, 480.36 g of 2-chloro-5-nitrobenzotrifluoride was obtained as a yellow oil. The yield was 96.13% and the purity was 99.29%.

References[1] SUN DAL KIM . Soluble polyimides with trifluoromethyl pendent groups[J]. Polymer, 2013. DOI:10.1016/j.polymer.2013.08.057.
Tag:2-Chloro-5-nitrobenzotrifluoride(777-37-7) Related Product Information
DINITROTOLUENE 3-Fluorobenzotrifluoride Ethylbenzene 4-Nitrotoluene 2-Methylbenzotrifluoride 2-Chloro-5-trifluoromethylpyridine Allylbenzene Benzotrifluoride 2-Nitrotoluene Chlorobenzene 3-Nitrotoluene 2-Chloro-5-nitrotoluene Benzene Sorafenib IMpurity Phenol, 4-(hydroxyamino)- 2-Chlorobenzotrifluoride 2-Pyridinecarboxamide,N-methyl-(9CI) Methyl 4-chloropicolinate

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