6316-07-0

Basic information

• Product Name: N-(2,2,2-trichloro-1-hydroxyethyl)benzamide
• Synonyms: benzamide, N-(2,2,2-trichloro-1-hydroxyethyl)-
• CAS NO: 6316-07-0
• Molecular Formula: C₉H₈Cl₃NO₂
• Molecular Weight: 268.5243
• Mol File: 6316-07-0.mol

Chemical Properties

• Boiling Point: 414.3°C at 760 mmHg
• Flash Point: 204.4°C
• Density: 1.505g/cm³
• Vapor Pressure: 1.32E-07mmHg at 25°C
• Refractive Index: 1.593
• CAS DataBase Reference: N-(2,2,2-trichloro-1-hydroxyethyl)benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2,2,2-trichloro-1-hydroxyethyl)benzamide(6316-07-0)
• EPA Substance Registry System: N-(2,2,2-trichloro-1-hydroxyethyl)benzamide(6316-07-0)

Safety Data

• Hazardous Substances Data: 6316-07-0(Hazardous Substances Data)

Upstream product

• 55-21-0 benzamide 
• 75-87-6 chloral 
• 302-17-0 chloral hydrate 
• 100-47-0 benzonitrile 
• 79-01-6 Trichloroethylene 
• 22180-78-5 N,N-dichloro-benzamide 
• 7647-01-0 hydrogenchloride 

Downstream Products

• 6780-31-0 2-acetoxy-2-benzoylamino-1,1,1-trichloro-ethane 
• 51361-23-0 N-(2,2,2-trichloro-1-methoxyethyl)benzamide 
• 63499-50-3 3-benzoyl-2-trichloromethyl-oxazolidine-4,5-dione 
• 6776-51-8 2,2,2-Trifluor-2',2',2'-trichlor-1,1'-bis-benzamino-diethylether 
• 6798-35-2 N-(1,2,2,2-tetrachloroethyl)benzamide 
• 134219-50-4 N-[2,2,2-Trichloro-1-(4-ethyl-phenyl)-ethyl]-benzamide 
• 77429-35-7 N-[2,2,2-Trichloro-1-(2,2-dichloro-1-phenyl-ethylamino)-ethyl]-benzamide 
• 29431-43-4 N-2,2-dichlorovinylbenzamide 
• 58956-79-9 N-(2,2-dichloro-1-hydroxy-ethyl)-benzamide 
• 49837-70-9 2-benzoylamino-3,3-dichloroacrylonitrile 
• 909798-35-2 C₁₆H₁₃ClN₄OS 
• 305331-23-1 C₁₆H₁₀Cl₂N₂OS 
• 10408-52-3 (rac)-2-(4-ethylphenyl)-2-hydroxyacetic acid 
• 6776-62-1 1,1,1-trichloro-2-amino-2-(benzamido)ethane 

Relevant articles and documents

Synthesis of New 1Н-Pyrrolo[3,4-с]pyridine-1,3(2Н)-diones

Abstract: A method for the synthesis of a series of new substituted 1H-pyrrolo[3,4-c]pyridine-1,3(2H)-diones was proposed based on the Diels–Alder type reaction of 4-methoxy-1,3-oxazoles with maleimide derivatives.

Novel 2H-1,3-benzoxazine ring formation by intramolecular heterocyclization of N-(α-aryloxyalkyl)imidoyl chlorides

A convenient synthetic approach to derivatives of 2-trichloromethyl and 2-dichlorometylene-2H-1,3-benzoxazines, based on intramolecular heterocyclization of readily accessible N-(α-aryloxytrichloroethyl)imidoyl chlorides, was developed. Base induced dehyd

A facile synthesis of 1,3-thiazole-4-sulfonyl chlorides

(Chemical Equation Presented) A four-step preparative-scale synthesis of eight 2-alkyl- and arylsubstituted thiazole-4-sulfonyl chlorides from chloralamides is reported. Good yields and easy availability of starting materials are valuable advantages of the procedure that gives access to formerly unattainable building blocks. Copyright Taylor & Francis Group, LLC.

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Sml2-mediated facile syntheses of N(2,2-dichlorovinyl)amides from acetates of chloralamide

Samarium diiodide-mediated elimination reaction provides a simple and general method to synthesise N-(2, 2-dichlorovinyl)amides 4 from acetates of chloralamides 3 in excellent yields. This novel reaction proceeds readily within a few minutes at room tempe

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REACTION OF N,N-DICHLOROAMIDES WITH TRICHLOROETHYLENE

The reaction of N,N-dichloroacetamide and N,N-dichlorobenzamide with trichloroethylene in an inert atmosphere leads to the formation of the products from the transformation of the corresponding acylimines of chloral, i.e. 2,2,2-trichloro-1,1-di(acetamido)benzamido ethanes, N-(2,2,2-trichloro-1-hydroxyethyl)acetamides and the corresponding benzamides, and pentachloroethane.In the reaction of N,N-dichlorobenzamide with trichloroethylene in the presence of atmospheric oxygen N-(dichloroacetyl)benzamide is obtained in additon to N-(2,2,2-trichloro-1-hydroxyethyl)benzamide and pentachloroethane.Its formation results from the parallel processes of oxidation of the trichloroethylene to dichloroacetyl chloride and reduction of the dichlorobenzamide to benzamide and their reaction.