295788-93-1

Basic information

• Product Name: Benzene, 1-bromo-2,4-bis(methoxymethoxy)-
• CAS NO: 295788-93-1
• Molecular Formula: C10H13BrO4
• Molecular Weight: 277.115
• Mol File: 295788-93-1.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: Benzene, 1-bromo-2,4-bis(methoxymethoxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-bromo-2,4-bis(methoxymethoxy)-(295788-93-1)
• EPA Substance Registry System: Benzene, 1-bromo-2,4-bis(methoxymethoxy)-(295788-93-1)

Safety Data

• Hazardous Substances Data: 295788-93-1(Hazardous Substances Data)

Upstream product

• 6626-15-9 4-Bromoresorcinol 
• 122776-88-9 (methoxymethoxy)methyl chloride 
• 107-30-2 chloromethyl methyl ether 

Downstream Products

• 704912-95-8 1-(2,4-bis-methoxymethoxy-phenyl)-3-(3-{4-[3-(2,4-bis-methoxymethoxy-phenyl)-3-hydroxy-propyl]-2-methoxy-phenoxy}-4-methoxymethoxy-phenyl)-propan-1-ol 
• 296764-08-4 3-[2,4-Bis(methoxymethoxy)phenyl]-2-cyclopenten-1-one 
• 1228321-25-2 4-(2,4-bis(methoxymethoxy)phenyl)tetrahydrothiopyran-4-ol 
• 1228321-33-2 3-(2,4-bis(methoxymethoxy)phenyl)tetrahydrothiophen-3-ol 
• 863578-46-5 2,4-bis(methoxymethoxy)phenylboronic acid 

Relevant articles and documents

Total synthesis of the novel benzophenone NP-011694

We report the total synthesis of NP-011694, a previously unreported fungal fermentation product from Analyticon Gmbh. The convergent synthesis employs Turbo Grignard and lithiation strategies, along with novel conditions for the simultaneous removal of mu

NOVEL 4-(HETEROCYCLOALKYL)BENZENE-1,3-DIOL COMPOUNDS AS TYROSINASE INHIBITORS, PROCESS FOR THE PREPARATION THEREOF AND USE THEREOF IN HUMAN MEDICINE AND ALSO IN COSMETICS

The present invention relates to novel 4- (heterocycloalkyl) benzene- 1,3-diol compounds corresponding to general formula (I) below: to the compositions containing same, to the process for the preparation thereof and to the use thereof in pharmaceutical or cosmetic compositions for use in the treatment or prevention of pigmentary disorders

Benzopyrans as selective estrogen receptor β agonists (SERBAs). Part 2: Structure-activity relationship studies on the benzopyran scaffold

Benzopyrans are selective estrogen receptor (ER) β agonists (SERBAs), which bind the ER subtypes α and β in opposite orientations. Here we describe structure-activity relationship studies that led to the discovery of bezopyran 5b. X-ray crystal structures