107558-73-6

Basic information

• Product Name: diethyl 2-(3-broMobenzyl)Malonate
• Synonyms: diethyl 2-(3-broMobenzyl)Malonate;RHFBUOOSCRTDLX-UHFFFAOYSA-N
• CAS NO: 107558-73-6
• Molecular Formula: C₁₄H₁₇BrO₄
• Molecular Weight: 329.18638
• Mol File: 107558-73-6.mol

Chemical Properties

• Boiling Point: 375.713°C at 760 mmHg
• Flash Point: 181.025°C
• Appearance: /
• Density: 1.345g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.523
• PKA: 12.41±0.59(Predicted)
• CAS DataBase Reference: diethyl 2-(3-broMobenzyl)Malonate(CAS DataBase Reference)
• NIST Chemistry Reference: diethyl 2-(3-broMobenzyl)Malonate(107558-73-6)
• EPA Substance Registry System: diethyl 2-(3-broMobenzyl)Malonate(107558-73-6)

Safety Data

• Hazardous Substances Data: 107558-73-6(Hazardous Substances Data)

Usage

InChI:InChI=1/C14H17BrO4/c1-3-18-13(16)12(14(17)19-4-2)9-10-6-5-7-11(15)8-10/h5-8,12H,3-4,9H2,1-2H3

Upstream product

• 823-78-9 meta-bromobenzyl bromide 
• 68-12-2 N,N-dimethyl-formamide 
• 105-53-3 diethyl malonate 
• 932-77-4 3-bromobenzyl chloride 
• 15852-73-0 (3-Bromophenyl)methanol 

Downstream Products

• 1608506-15-5 C₁₇H₂₀BrNO₄ 
• 1608506-61-1 C₁₂H₁₄BrN₃O₂ 
• 1608506-51-9 C₁₂H₁₃BrN₄ 
• 1608506-31-5 C₁₂H₁₄BrNO 
• 1608506-23-5 C₁₄H₁₆BrNO₂ 
• 1608506-71-3 C₁₂H₁₃BrClN₃O 
• 377732-56-4 2-(3-Bromobenzyl)-1,3-propanediol 
• 70146-78-0 diethyl 2-(4-bromobenzyl)malonate 
• 454685-23-5 4,6-diiodo-5-(3-bromobenzyl)pyrimidine 
• 454685-24-6 4-amino-6-iodo-5-(3-bromobenzyl)pyrimidine 
• 454685-22-4 4,6-dichloro-5-(3-bromobenzyl)pyrimidine 
• 335159-82-5 3-(m-bromophenyl)propionyl chloride 
• 42287-90-1 3-(3-bromophenyl)propanoic acid 
• 34598-49-7 5-Bromo-1-indanone 

Relevant articles and documents

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The article describes a general procedure for synthesizing hydantoins of the indan series, which makes it possible to obtain bioisosteric analogs of 1-aminoindan-1,5-dicarboxylic acid, a group I metabotropic glutamate receptor antagonist.

Biocatalytic Desymmetrization of Prochiral 3-Aryl and 3-Arylmethyl Glutaramides: Different Remote Substituent Effect on Catalytic Efficiency and Enantioselectivity

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