138116-09-3

Basic information

• Product Name: Benzaldehyde, 2-(acetyloxy)-5-bromo-
• CAS NO: 138116-09-3
• Molecular Formula: C9H7BrO3
• Molecular Weight: 243.057
• Mol File: 138116-09-3.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Benzaldehyde, 2-(acetyloxy)-5-bromo-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzaldehyde, 2-(acetyloxy)-5-bromo-(138116-09-3)
• EPA Substance Registry System: Benzaldehyde, 2-(acetyloxy)-5-bromo-(138116-09-3)

Safety Data

• Hazardous Substances Data: 138116-09-3(Hazardous Substances Data)

Upstream product

• 108-24-7 acetic anhydride 
• 1761-61-1 5-bromosalicyclaldehyde 

Relevant articles and documents

Development of 6-arylcoumarins as nonsteroidal progesterone antagonists. Structure–activity relationships and fluorescence properties

Progesterone is involved in multiple physiological processes, including female reproduction, via binding to the progesterone receptor (PR). We have developed 6-arylcoumarins such as 5 and 6 as non-steroidal PR antagonists with receptor-binding-dependent f

Copper(I)-catalyzed hydroalkoxylation/hydrogen-bonding-induced asymmetric hetero-diels-alder cycloaddition cascade: An approach to aromatic spiroketals

One thing leads to another: Bis(benzannelated) 5,6-spiroketal skeletons can be constructed by an efficient cascade process involving an unprecedented CuI-catalyzed intramolecular alkyne hydroalkoxylation and an asymmetric hetero-Diels-Alder cyc

Convenient synthesis of a simple coumarin from salicylaldehyde and wittig reagent. IV: Improved synthetic method of substituted coumarins

The reaction of salicylaldehydes (2) with Horner-Wadsworth-Emmons (HWE) or Ando-HWE reagents was attempted to afford intramolecular phosphonate derivatives (6). A new synthetic method for coumarins (1) was achieved by using protected 2.