92989-59-8

Basic information

• Product Name: (3,5-dimethoxyphenyl)(2-phenyl-[1,3]-dithian-2-yl)-methanol
• Synonyms: (3,5-dimethoxyphenyl)(2-phenyl-[1,3]-dithian-2-yl)-methanol
• CAS NO: 92989-59-8
• Molecular Weight: 362.514
• Mol File: 92989-59-8.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: (3,5-dimethoxyphenyl)(2-phenyl-[1,3]-dithian-2-yl)-methanol(CAS DataBase Reference)
• NIST Chemistry Reference: (3,5-dimethoxyphenyl)(2-phenyl-[1,3]-dithian-2-yl)-methanol(92989-59-8)
• EPA Substance Registry System: (3,5-dimethoxyphenyl)(2-phenyl-[1,3]-dithian-2-yl)-methanol(92989-59-8)

Safety Data

• Hazardous Substances Data: 92989-59-8(Hazardous Substances Data)

Upstream product

• 100-52-7 benzaldehyde 
• 5425-44-5 2-Phenyl-[1,3]dithiane 
• 7311-34-4 3,5-dimethoxybenzaldehdye 

Downstream Products

• 34911-33-6 5,7-Dimethoxy-2-phenylbenzofuran 
• 1354492-73-1 (2S)-amino-5-[(RS)-1-(3,5-dimethoxyphenyl)-2-oxo-2-phenylethoxy]-5-oxopentanoic acid hydrochloride 
• 1353745-58-0 (S)-1-tert-butyl 5-[(RS)-1-(3,5-dimethoxyphenyl)-2-oxo-2-phenylethyl] 2-(tert-butoxycarbonylamino)pentanedioate 
• 1353745-52-4 (RS)-1-(3,5-dimethoxyphenyl)-2-oxo-2-phenylethyl 4-aminobutanoate hydrochloride 
• 1353745-57-9 (RS)-1-(3,5-dimethoxyphenyl)-2-oxo-2-phenylethyl 4-(tert-butoxycarbonylamino)butanoate 
• 457612-13-4 adipic acid (4,5-dimethoxy-2-nitrobenzyl) ester (3',5'-dimethoxybenzoin) ester 
• 457612-12-3 glutaric acid (4,5-dimethoxy-2-nitrobenzyl) ester (3',5'-dimethoxybenzoin) ester 
• 457612-11-2 succinic acid (4,5-dimethoxy-2-nitrobenzyl) ester (3',5'-dimethoxybenzoin) ester 
• 457612-10-1 malonic acid (4,5-dimethoxy-2-nitrobenzyl) ester (3',5'-dimethoxybenzoin) ester 
• 457612-09-8 oxalic acid (4,5-dimethoxy-2-nitrobenzyl) ester (3',5'-dimethoxybenzoin) ester 
• 1027437-02-0 heptanedioic acid mono-[1-(3,5-dimethoxy-phenyl)-2-oxo-2-phenyl-ethyl] ester 
• 457612-26-9 adipic acid (3',5'-dimethoxybenzoin) ester methyl ester 
• 1027171-77-2 pentanedioic acid mono-[1-(3,5-dimethoxy-phenyl)-2-oxo-2-phenyl-ethyl] ester 

Relevant articles and documents

Modulated photochemical reactivities of: O -acetylated (3′,5′-dimethoxyphenyl)heteroaryl acyloin derivatives under direct irradiation and photo-induced electron transfer conditions

3′,5′-Dimethoxybenzoin esters are important photoremovable protecting groups which form 2-phenylbenzofuran derivatives upon photo-release. We utilized a similar concept to test a photochemical method of installing a benzofuran moiety to the conjugated bac

A time-resolved spectroscopic study of the bichromophoric phototrigger 3',5'-dimethoxybenzoin diethyl phosphate: Interaction between the two chromophores determines the reaction pathway

3',5'-Dimethoxybenzoin (DMB) is a bichromophoric system that has widespread application as a highly efficient photoremovable protecting group (PRPG) for the release of diverse functional groups. The photodeprotection of DMB phototriggers is remarkably cle

Design, synthesis, and photochemical properties of a photoreleasable ubiquinol-2: A novel compound for studying rapid electron-transfer kinetics in ubiquinol-oxidizing enzymes

The design and multistep convergent synthesis of the novel photoactive ubiquinol-benzoin adduct 1a,b has been accomplished. Optical spectra of the steady-state photolysis reactions showed a smooth conversion from 1a,b to 5,7-dimethoxy-2-phenylbenzofuran (13) and ubiquinol-2 with an isobestic point at 258 nm. HPLC analysis of the photoproducts was also consistent with the clean formation of the desired ubiquinol-2 (3) and the expected 5,7-dimethoxy-2-phenylbenzofuran (2). Transient photolysis at 355 nm was consistent with a rapid photolysis rate that exceeded the instrument response time (> 106 s-1). Accordingly, the study of rapid electron-transfer events in ubiquinol oxidizing enzymes is now feasible. Furthermore, the synthetic methods developed herein will be of general application for the facile synthesis of a variety of photoreleasable substrates for studying rapid kinetic events in enzymatic reactions.