34243-53-3

Basic information

• Product Name: Benzamide, 4-bromo-N-(2,2,2-trichloro-1-hydroxyethyl)-
• CAS NO: 34243-53-3
• Molecular Formula: C9H7BrCl3NO2
• Molecular Weight: 347.423
• Mol File: 34243-53-3.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Benzamide, 4-bromo-N-(2,2,2-trichloro-1-hydroxyethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzamide, 4-bromo-N-(2,2,2-trichloro-1-hydroxyethyl)-(34243-53-3)
• EPA Substance Registry System: Benzamide, 4-bromo-N-(2,2,2-trichloro-1-hydroxyethyl)-(34243-53-3)

Safety Data

• Hazardous Substances Data: 34243-53-3(Hazardous Substances Data)

Upstream product

• 698-67-9 p-bromobenzamide 
• 75-87-6 chloral 

Downstream Products

• 71418-32-1 4-bromo-N-(1,2,2,2-tetrachloroethyl)benzamide 
• 54888-32-3 N-(2,2-dichloroethenyl)-4-bromobenzamide 
• 1221723-38-1 2-(4-bromophenyl)-1,3-thiazole-4-sulfonyl chloride 
• 1382676-43-8 4-benzylsulfanyl-2-(4-bromophenyl)-1,3-thiazole 
• 1382676-13-2 N-(1-benzylsulfanyl-2,2-dichloroethyl)-4-bromobenzamide 
• 1265593-61-0 4-bromo-N-(2,2,2-trichloro-1-(6-chloropyridin-3-ylamino)ethyl)benzamide 
• 110968-62-2 (4-Bromo-phenyl)-(3-trichloromethyl-2-aza-bicyclo[2.2.1]hept-5-en-2-yl)-methanone 
• 60600-34-2 N-p-Brombenzoyl-chloralimin 

Relevant articles and documents

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.

SELECTIVE SPHINGOSINE-1-PHOSPHATE RECEPTOR ANTAGONISTS

Described herein are compounds of the formula useful as antagonists of sphingosine-1- phosphate receptors. Further described herein is the use of these compounds and related pharmaceutical compositions to treat disorders associated with sphingosine-1 -pho

Synthese von Heterocyclen durch Cycloaddition; Synthesen und Umsetzung neuer Azanorbornene

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