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
• Article Data: 10

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 
• 7647-01-0 hydrogenchloride 
• 79-01-6 Trichloroethylene 
• 22180-78-5 N,N-dichloro-benzamide 

Downstream Products

• 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 
• 63499-64-9 Malonic acid bis-(1-benzoylamino-2,2,2-trichloro-ethyl) ester 
• 29431-43-4 N-2,2-dichlorovinylbenzamide 
• 6780-31-0 2-acetoxy-2-benzoylamino-1,1,1-trichloro-ethane 
• 49837-70-9 2-benzoylamino-3,3-dichloroacrylonitrile 
• 6780-37-6 N-(benzoyl)trichloroacetaldimine 
• 110968-60-0 Phenyl-(3-trichloromethyl-2-aza-bicyclo[2.2.1]hept-5-en-2-yl)-methanone 
• 64390-65-4 N-[2,2,2-trichloro-1-[(chloroacetyl)-amino]-ethyl]-benzamide 
• 55630-07-4 <1-(benzoylamino)-2,2-dichlorovinyl>triphenylphosphonium chloride 

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.

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.

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