19358-41-9

Basic information

• Product Name: 2-CHLOROPHENYL CHLOROFORMATE
• Synonyms: 2-CHLOROPHENYL CHLOROFORMATE;ChloroforMic acid o-chlorophenyl ester;o-Chlorophenyl chloroforMate;2-chlorophenyl carbonochloridate
• CAS NO: 19358-41-9
• Molecular Formula: C₇H₄Cl₂O₂
• Molecular Weight: 191.01
• Product Categories: Acid Halides;Carbonyl Compounds;Organic Building Blocks
• Mol File: 19358-41-9.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 221 °C(lit.)
• Flash Point: 230 °F
• Appearance: /
• Density: 1.37 g/mL at 25 °C(lit.)
• Vapor Pressure: 0.75 psi ( 20 °C)
• Refractive Index: n20/D 1.526(lit.)
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 2-CHLOROPHENYL CHLOROFORMATE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-CHLOROPHENYL CHLOROFORMATE(19358-41-9)
• EPA Substance Registry System: 2-CHLOROPHENYL CHLOROFORMATE(19358-41-9)

Safety Data

• Hazard Codes: T
• Statements: 23/24/25-34
• Safety Statements: 23-26-36/37/39-45
• RIDADR: UN 3277 6.1/PG 2
• WGK Germany: 3
• Hazardous Substances Data: 19358-41-9(Hazardous Substances Data)

Usage

General Description

2-Chlorophenyl chloroformate is a chemical compound with the formula C7H4Cl2O2. It is a colorless to pale yellow liquid with a pungent odor, and it is used as a reagent in organic synthesis. Its main industrial applications include the production of pharmaceuticals, agrochemicals, and other specialty chemicals. It is also used as an intermediate in the manufacturing of dyes, polymers, and resins. 2-Chlorophenyl chloroformate is a highly reactive compound and must be handled with caution due to its corrosive and irritating properties. It is also toxic if ingested or inhaled, with potential harmful effects to the respiratory and nervous systems.

InChI:InChI=1/C7H4Cl2O2/c8-5-3-1-2-4-6(5)11-7(9)10/h1-4H

Upstream product

• 32315-10-9 bis(trichloromethyl) carbonate 
• 95-57-8 2-monochlorophenol 
• 75-44-5 phosgene 

Downstream Products

• 132983-13-2 carbonic acid-(5-acetyl-[8]quinolyl ester)-(2-chloro-phenyl ester) 
• 97611-33-1 2-chlorophenyl carbamate 
• 68621-30-7 (3-nitro-phenyl)-carbamic acid-(2-chloro-phenyl ester) 
• 42571-48-2 ar double bond & ligand) 
• 42571-51-7 C₁₅H₁₃ClN₂O₂ 
• 42571-44-8 C₁₆H₁₅ClN₂O₂ 
• 42571-47-1 C₁₅H₁₂Cl₂N₂O₂ 
• 42571-45-9 C₁₇H₁₇ClN₂O₂ 
• 42571-46-0 C₁₆H₁₄Cl₂N₂O₂ 
• 42571-49-3 C₁₆H₁₄Cl₂N₂O₂ 
• 929281-37-8 2-chlorophenyl [2-((4-{[(2,4-dichlorophenyl)sulfonyl]amino}butyl){[(1-methylethyl)amino]carbonyl}amino)ethyl]carbamate 
• 889857-41-4 2-chlorophenyl 6-(5-chloro-2-methoxybenzyl)-3,7-dioxo-4-(2,4,6-trimethoxybenzyl)-1,4-diazepan-1-carboxylate 

Relevant articles and documents

An easy procedure for synthesis of 1,3,4-oxadiazines: A potential antimicrobial agents

An efficient and accessible procedure for the synthesis of 1,3,4-oxadiazines was developed. Reaction involves the cyclocondensation of phenylhydrazones catalyzed by a mild base triethylamine to produce 1,3,4-oxadiazines in good yields. The synthesized new

Preparation of chloroformates using bis(trichloromethyl)carbonate

The synthesis of eight chloroformates using bis(trichloromethyl) carbonate(BTC) is reported. It has been found that the yields by this BTC method are improved over the earlier phosgene method, and sodium hydroxide is better than pyridine as catalyst for the preparation of phenyl chloroformate.