3787-28-8

Basic information

• Product Name: 2,3,3-TRICHLOROPROPENAL
• Synonyms: 2,3,3-TRICHLOROPROPENAL
• CAS NO: 3787-28-8
• Molecular Formula: C₃HCl₃O
• Molecular Weight: 159.39
• Mol File: 3787-28-8.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 222.6°C (rough estimate)
• Flash Point: 71.1°C
• Appearance: /
• Density: 1.7293 (rough estimate)
• Vapor Pressure: 0.689mmHg at 25°C
• Refractive Index: 1.4861 (estimate)
• CAS DataBase Reference: 2,3,3-TRICHLOROPROPENAL(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3,3-TRICHLOROPROPENAL(3787-28-8)
• EPA Substance Registry System: 2,3,3-TRICHLOROPROPENAL(3787-28-8)

Safety Data

• Hazardous Substances Data: 3787-28-8(Hazardous Substances Data)

Usage

Safety Profile

Poison by intraperitoneal route.Mutation data reported. When heated to decomposition itemits toxic fumes of Clí.

InChI:InChI=1/C3HCl3O/c4-2(1-7)3(5)6/h1H

Upstream product

• 1600-37-9 1,1,2,3,3-pentachloro-1-propene 
• 1561-37-1 3-butoxy-1,1,3-trichloro-propene 
• 21400-41-9 1,1,2,4,4-pentachloro-1,3-butadiene 
• 53356-86-8 1,1,2-trichloro-3,3-diethoxy-propene 

Downstream Products

• 98137-90-7 (2,3,3-trichloro-prop-2-enylidene)-malononitrile 
• 590-29-4 potassium formate 
• 79-01-6 Trichloroethylene 
• 136689-12-8 2,3,3-trichloropropenal tosylhydrazone 
• 126725-09-5 (S)-2-Amino-4-[(R)-1-(carboxymethyl-carbamoyl)-2-((E)-1,2-dichloro-3-oxo-propenylsulfanyl)-ethylcarbamoyl]-butyric acid 
• 126725-10-8 (S)-2-Amino-4-[(R)-2-{1-[(R)-2-((S)-4-amino-4-carboxy-butyrylamino)-2-(carboxymethyl-carbamoyl)-ethylsulfanyl]-2-chloro-3-oxo-propenylsulfanyl}-1-(carboxymethyl-carbamoyl)-ethylcarbamoyl]-butyric acid 
• 20883-09-4 2,3-Dichlor-3-phenoxy-acrolein 
• 65480-63-9 2-Chloro-3,3-bis-phenylsulfanyl-propenal 
• 65480-65-1 (E)-2,3-Dichloro-3-phenylsulfanyl-propenal 
• 815-58-7 2,3,3-trichloroacryloyl chloride 
• 3533-68-4 (2Z)-2,3-dichloroprop-2-enoic acid 
• 1600-37-9 1,1,2,3,3-pentachloro-1-propene 
• 1769-47-7 α-(1,2,2-Trichlorethenyl)benzolmethanol 
• 1733-27-3 1,1,2-Trichlor-5-phenyl-pent-1-en-4-in-3-ol 

Relevant articles and documents

Chemistry of polyhalogenated nitrobutadienes, part 9: Acyclic and heterocyclic nitroenamines and nitroimines from 2-nitroperchlorobuta-1,3-diene

Various amino, diamino, aminothio, or benzotriazolo compounds derived from the exceedingly versatile 2-nitroperchlorobutadiene (1) gave structurally interesting and physiologically promising nitro-enamines,-imines,-amidines, and hydrazines as well as ring closure reaction products, e. g. pyrimidines and pyrazoles. Most of these reactions turned out to be highly selective with good to very good yields. The structure of the pyrazole precursor (E,E)-1-(benzotriazol-1-yl)-4,4-dichloro-3-(4-ethoxyphenylamino) -1-(4-ethoxyphenylimino)-2-nitrobut-2-ene (30), due to its exceptional substitution pattern, was evidenced by single-crystal X-ray diffraction analysis.