34328-46-6

Basic information

• Product Name: 4-Chloro-3-(trifluoromethyl)benzaldehyde
• Synonyms: TIMTEC-BB SBB003468;4-CHLORO-3-(TRIFLUOROMETHYL)BENZALDEHYDE;3-Trifluoromethyl-4-Chlorobenzaldehyde;4-Chloro-3-(trifluoromethyl)benzaldehyde, 97+%;4-Chloro-3-(trifluoromethyl)benzaldehyde 98%;4-Chloro-3-(trifluoromethyl)benzaldehyde98%;2-Chloro-5-formylbenzotrifluoride;4-chloro-3-trifluorobenzaldehyde
• CAS NO: 34328-46-6
• Molecular Formula: C₈H₄ClF₃O
• Molecular Weight: 208.56
• EINECS: 251-940-5
• Product Categories: Aromatic Aldehydes & Derivatives (substituted);Benzaldehyde;Aldehydes;C8;Carbonyl Compounds;Fluorine series
• Mol File: 34328-46-6.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 218 °C(lit.)
• Flash Point: 227 °F
• Appearance: Clear colorless/Liquid
• Density: 1.45 g/mL at 25 °C(lit.)
• Vapor Pressure: 0.105mmHg at 25°C
• Refractive Index: n20/D 1.504(lit.)
• Storage Temp.: Keep in dark place,Sealed in dry,Room Temperature
• Sensitive: Air Sensitive
• BRN: 2101897
• CAS DataBase Reference: 4-Chloro-3-(trifluoromethyl)benzaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Chloro-3-(trifluoromethyl)benzaldehyde(34328-46-6)
• EPA Substance Registry System: 4-Chloro-3-(trifluoromethyl)benzaldehyde(34328-46-6)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36
• WGK Germany: 3
• HazardClass: IRRITANT
• Hazardous Substances Data: 34328-46-6(Hazardous Substances Data)

Usage

Chemical Properties

Clear colorless liquid

Uses

4-Chloro-3-(trifluoromethyl)benzaldehyde is an important raw material and intermediate used in organic synthesis, pharmaceuticals agrochemicals and dyestuff fields.

General Description

4-Chloro-3-(trifluoromethyl)benzaldehyde is a benzaldehyde derivative. Its enthalpy of vaporization at boiling point has been reported.

InChI:InChI=1/C8H4ClF3O/c9-7-2-1-5(4-13)3-6(7)8(10,11)12/h1-4H

Upstream product

• 445-01-2 5-bromo-2-chlorobenzotrifluoride 
• 144155-72-6 4--1-chloro-2-(trifluoromethyl)benzene 
• 75-17-2 formaldoxime 
• 320-51-4 4-chloro-3-trifluoromethyl-aniline 

Downstream Products

• 144128-81-4 5-(4-Chloro-3-trifluoromethyl-phenyl)-cyclohexane-1,3-dione 
• 144155-23-7 7-Chloro-3-(4-chloro-3-trifluoromethyl-phenyl)-3,4-dihydro-2H,10H-acridine-1,9-dione 
• 144155-52-2 7-Chloro-3-(4-chloro-3-trifluoromethyl-phenyl)-1-[(E)-3-dimethylamino-propylimino]-1,3,4,10-tetrahydro-2H-acridin-9-one 
• 144155-81-7 Sodium; 5-(4-chloro-3-trifluoromethyl-phenyl)-6-ethoxycarbonyl-3-oxo-cyclohex-1-enolate 
• 132605-01-7 4-chloro-3-trifluoromethyl-cinnamonitrile 
• 65735-71-9 (4-chloro-3-(trifluoromethyl)phenyl)methanol 
• 1314510-19-4 C₂₄H₁₉ClF₃N₃O 
• 1221962-33-9 4-(5-chloro-2-benzimidazolyl)-3-(4-chloro-3-trifluoromethylphenyl)butanoic acid hydrochloride 
• 1221962-34-0 3-(4-chloro-3-trifluoromethylphenyl)glutaric anhydride 
• 1442690-92-7 (2E)-1-(3',4',5'-trimethoxyphenyl)-3-(3-trifluoromethyl-4-chlorophenyl)-2-propen-1-one 

Relevant articles and documents

Process for producing trifluoromethylbenzylamines

The present invention relates to a process for producing a trifluoromethylbenzylamine represented by the general formula (1). This process includes the step of reducing an oxime represented by the general formula (2), where R1represents hydrogen atom, a halogen atom selected from the group consisting of fluorine, chlorine, bromine and iodine, or trifluoromethyl group, where R1is defined as above, and R2represents hydrogen atom, an alkyl group or an aralkyl group. With this process, the trifluoromethylbenzylamine can be produced with high selectivity.