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

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

Uses

Used in Pharmaceutical Industry:
2-Chlorophenyl chloroformate is utilized as a key intermediate in the synthesis of various pharmaceuticals. Its reactivity allows for the creation of a wide range of drug molecules, contributing to the development of new medications and therapies.
Used in Agrochemical Industry:
In the agrochemical sector, 2-Chlorophenyl chloroformate serves as an essential component in the production of pesticides and other crop protection agents. Its role in these applications helps to enhance crop yields and protect plants from harmful pests and diseases.
Used in Specialty Chemicals Production:
2-CHLOROPHENYL CHLOROFORMATE is also employed in the manufacturing of specialty chemicals, which are used in a variety of applications, including but not limited to, the production of dyes, polymers, and resins. Its versatility in chemical reactions makes it a valuable asset in this industry.
Used as a Chemical Intermediate in Dye, Polymer, and Resin Manufacturing:
2-Chlorophenyl chloroformate is used as a reactive intermediate in the synthesis of dyes, polymers, and resins. Its involvement in these processes is crucial for the development of new materials with specific properties required for various industrial applications.

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

Upstream product

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

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 
• 84043-59-4 1-[2-(2-Chloro-phenoxy)-acetyl]-3-(5-phenyl-[1,3,4]oxadiazol-2-yl)-thiourea 
• 84043-62-9 1-[2-(2-Chloro-phenoxy)-acetyl]-3-[5-(4-chloro-phenyl)-[1,3,4]oxadiazol-2-yl]-thiourea 
• 84052-73-3 1-[2-(2-Chloro-phenoxy)-acetyl]-3-[5-(3,5-dibromo-2-hydroxy-phenyl)-[1,3,4]oxadiazol-2-yl]-thiourea 
• 193139-59-2 4-(tert-Butyl-dimethyl-silanyloxymethyl)-2-ethynyl-2H-quinoline-1-carboxylic acid 2-chloro-phenyl ester 

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

AZETIDINE DERIVATIVES USEFUL FOR THE TREATMENT OF METABOLIC AND INFLAMMATORY DISEASES

Compounds are disclosed that have a formula represented by the following: These compounds may be prepared as a pharmaceutical composition, and may be used for the prevention and treatment of a variety of conditions in mammals including humans, including by way of non-limiting example inflammatory conditions, infectious diseases, autoimmune diseases, diseases involving impairment of immune cell functions, cardiometabolic diseases, and/or proliferative diseases.

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.

Heat-sensitive recording materials and phenol compounds

Heat-sensitive recording materials contain an electron-donating chromogenic compound and an electron-attracting compound. The recording materials also contain at least one compound represented by the following formula: STR1 wherein R1 and R3 mean a hydrogen atom or an alkyl, aralkyl or aryl group, R2 and R4 denote an alkyl, alkenyl, aralkyl or aryl group, X1, X2, Y1 and Y2 stand for an oxygen or a sulfur atom, and --Z1 -- and --Z2 -- are a specific aromatic group. Also provided are phenol compounds represented by the following formula: STR2 wherein R1, R2, X1 and Y1 have the same meanings as defined above; R5 and R6 are a hydrogen or halogen atom or an alkyl, alkoxy, aralkyl, aryl or hydroxyl group; p and q stand for an integer of 1-4; R5 and R6 may be either the same or different when p and q represent an integer of 2 or greater; and --Z3 -- means a specific divalent group.