265299-12-5

Basic information

• Product Name: Benzenepropanoic acid, b-(acetyloxy)-2-bromo-a-methylene-, methyl ester
• CAS NO: 265299-12-5
• Molecular Formula: C13H13BrO4
• Molecular Weight: 313.148
• Mol File: 265299-12-5.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: Benzenepropanoic acid, b-(acetyloxy)-2-bromo-a-methylene-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenepropanoic acid, b-(acetyloxy)-2-bromo-a-methylene-, methyl ester(265299-12-5)
• EPA Substance Registry System: Benzenepropanoic acid, b-(acetyloxy)-2-bromo-a-methylene-, methyl ester(265299-12-5)

Safety Data

• Hazardous Substances Data: 265299-12-5(Hazardous Substances Data)

Upstream product

• 108-24-7 acetic anhydride 
• 352533-60-9 methyl 2-((2-bromophenyl)(hydroxy)methyl)acrylate 
• 6630-33-7 ortho-bromobenzaldehyde 
• 75-36-5 acetyl chloride 

Downstream Products

• 885612-66-8 2-aminomethyl-3-(2-bromophenyl)acrylic acid methyl ester 
• 1020105-37-6 C₁₉H₁₆BrNO₂ 
• 1020105-42-3 C₂₀H₁₈BrNO₂ 
• 1020105-39-8 C₂₀H₁₈BrNO₂ 
• 1020105-43-4 C₂₁H₂₀BrNO₂ 
• 1020105-40-1 C₂₀H₁₈BrNO₃ 
• 1020105-41-2 C₂₃H₂₂BrNO₄ 
• 1018071-82-3 C₂₁H₂₂BrNO₄S 
• 752254-58-3 methyl 2-(acetoxymethyl)-3-(2-bromophenyl)acrylate 
• 1155923-19-5 C₁₇H₁₆BrNO₂ 
• 1155922-90-9 C₁₈H₁₈BrNO₂ 
• 1189520-13-5 (E)-5-(2-bromobenzylidene)-2-(3-methoxyphenyl)-5,6-dihydropyrimidin-4(3H)-one 

Relevant articles and documents

SUBSTITUTED DIHYDROPYRAZOLO PYRAZINE CARBOXAMIDE DERIVATIVES

The invention relates to substituted dihydropyrazolo pyrazine carboxamide derivatives and to processes for their preparation, and also to their use for preparing medicaments for the treatment and/or prophylaxis of diseases, in particular cardiovascular disorders, preferably thrombotic or thromboembolic disorders, and diabetes, and also urogenital and ophthalmic disorders.

One-pot synthesis of allyl thioacetate from benzaldehydes and activated alkenes using the Morita-Baylis-Hillman reaction as a key step

An efficient, regioselective and steresoselecitive one-pot protocol for the synthesis of (Z)-S-2-alkoxycarbonyl-3-acylallyl ethanethioates and (E)-S-2-cyano-3-acylallyl ethanethioates from benzaldehydes and activated alkenes (methyl acrylate and acrylonit

N-bromosuccinimide-mediated radical cyclization of 3-arylallyl azides: Synthesis of 3-substituted quinolines

Visible light irradiation of N-bromosuccinimide serves as an effective means to convert methyl 2-(azidomethyl)-3-arylpropenoates and 2-(azidomethyl)-3-arylacrylonitriles to the corresponding iminyl radicals via ?±-hydrogen abstraction and subsequent extrusion of dinitrogen. Thus formed iminyl radicals then undergo intramolecular ortho attack on the aryl ring, affording methyl quin-oline-3-carboxylates and quinoline-3-carbonitriles respectively.