102586-01-6

Basic information

• Product Name: N-(2-Bromo-2-propenyl)benzamide
• Synonyms: N-(2-Bromo-2-propenyl)benzamide
• CAS NO: 102586-01-6
• Molecular Formula: C₁₀H₁₀BrNO
• Molecular Weight: 240.0965
• Mol File: 102586-01-6.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 348.7°Cat760mmHg
• Flash Point: 164.7°C
• Appearance: /
• Density: 1.45g/cm³
• Vapor Pressure: 4.95E-05mmHg at 25°C
• Refractive Index: 1.6
• CAS DataBase Reference: N-(2-Bromo-2-propenyl)benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-Bromo-2-propenyl)benzamide(102586-01-6)
• EPA Substance Registry System: N-(2-Bromo-2-propenyl)benzamide(102586-01-6)

Safety Data

• Hazardous Substances Data: 102586-01-6(Hazardous Substances Data)

Usage

InChI:InChI=1/C10H10BrNO/c1-7(11)6-8-4-2-3-5-9(8)10(12)13/h2-5H,1,6H2,(H2,12,13)

Upstream product

• 55-21-0 benzamide 
• 513-31-5 2-bromoallyl bromide 
• 6943-51-7 2-bromoallylamine 
• 98-88-4 benzoyl chloride 

Downstream Products

• 917092-14-9 N-(2-bromo-allyl)-N-methyl-benzamide 
• 54520-84-2 1-methyl-4-phenyl-pyrrolidin-2-one 
• 65178-52-1 N-allyl-N-methylbenzamide 
• 10283-95-1 N-allylbenzamide 
• 122279-62-3 N-(2-deuterioallyl)benzamide 
• 122279-63-4 N-(2-methylthioallyl)benzamide 
• 122279-66-7 N-(3-hydroxy-3-methyl-2-methylenebutyl)benzamide 
• 122279-64-5 N-(3-hydroxy-4-methyl-2-methylenepentyl)benzamide 
• 122279-65-6 N-(3-hydroxy-2-methylene-3-phenylpropyl)benzamide 
• 122279-67-8 N-(3-hydroxy-2-methylene-3,3-diphenylpropyl)benzamide 
• 1346241-00-6 C₁₅H₁₅NO 
• 1346241-05-1 C₁₅H₁₅NO 
• 1346241-01-7 C₁₈H₁₅NO 
• 1346241-06-2 C₁₈H₁₅NO 

Relevant articles and documents

A simple one-pot synthesis of 2-aryl-5-alkyl-Substituted oxazoles byCs 2CO3-Mediated Reactions of aromatic primary amides with 2,3-dibromopropene

A simple and efficient method for the synthesis of 2-aryl-5-alkyl- substituted oxazoles has been developed. A series of 2,5-disubstituted oxazoles were synthesized in a single step by Cs2CO3-mediated reactions of aromatic primary amides with 2,3-dibromopr

N-Substituted Lithium 2-Lithioallylamines: New Intermediates in Synthesis

N-Phenyl or N-benzoyl 2-halogenoallylamines (5) or (10) react successively with phenyl-lithium and lithium naphthalenide at -78 deg C to give the intermediates (4) or (11), which on reaction with electrophiles (water, deuterium oxide, dimethyl disulphide, aldehydes, ketones, or allyl bromide) yield functionalized allyl amines (6) and (12).The corresponding N-alkyl derivatives (9) afford prop-2-ynylamines (8) under the same reaction conditions.