63192-57-4

Basic information

• Product Name: 3,3-DIHYDROXYBENZYL
• Synonyms: 3,3-DIHYDROXYBENZYL;3,3''-Dihydroxybenzil
• CAS NO: 63192-57-4
• Molecular Formula: C₁₄H₁₀O₄
• Molecular Weight: 242.23
• Mol File: 63192-57-4.mol
• Article Data: 5

Chemical Properties

• Melting Point: 149-149.5 °C(Solv: water (7732-18-5); 1,2-dichloroethane (107-06-2))
• Boiling Point: 500.4±35.0 °C(Predicted)
• Appearance: /
• Density: 1.366±0.06 g/cm3(Predicted)
• PKA: 8.42±0.10(Predicted)
• CAS DataBase Reference: 3,3-DIHYDROXYBENZYL(CAS DataBase Reference)
• NIST Chemistry Reference: 3,3-DIHYDROXYBENZYL(63192-57-4)
• EPA Substance Registry System: 3,3-DIHYDROXYBENZYL(63192-57-4)

Safety Data

• Hazardous Substances Data: 63192-57-4(Hazardous Substances Data)

Upstream product

• 40101-17-5 3,3'-dimethoxybenzil 
• 626-02-8 3-Iodophenol 
• 388061-72-1 3-[2-(trimethylsilylethynyl)]phenol 
• 100-83-4 meta-hydroxybenzaldehyde 
• 63192-58-5 (1,2-bis(3-hydroxyphenyl)-2-hydroxyethanone) 

Downstream Products

• 1402074-85-4 C₄₆H₇₄O₄ 
• 1402074-82-1 C₃₈H₅₈O₄ 
• 1402074-84-3 C₄₂H₆₆O₄ 
• 1402074-83-2 C₄₀H₆₂O₄ 
• 1402074-80-9 C₃₄H₅₀O₄ 
• 1402074-81-0 C₃₆H₅₄O₄ 
• 63192-59-6 1,2,Bis(3-hydroxyphenyl)ethanone 
• 63192-58-5 (1,2-bis(3-hydroxyphenyl)-2-hydroxyethanone) 
• 58931-32-1 1,2-bis[3-(2-diethylaminoethoxy)phenyl]ethane-1,2-dione 

Relevant articles and documents

Synthesis of hydroxy benzoin/benzil analogs and investigation of their antioxidant, antimicrobial, enzyme inhibition, and cytotoxic activities

In this study, hydroxy benzoin (1-7), benzil (8-14), and benzoin/benzil-O-β-D-glucosides (15-25) were synthesized to investigate their biological activities. An efficient method for synthesizing hydroxy benzoin compounds (1-7) was prepared from four diffe

2,2-dimethoxy-1,2-DI[4-(meth)acryloyloxy]phenylethane-1-one, method for producing the same, radical polymerization initiator and photocurable composition

The invention provides 2,2-dimethoxy-1,2-di-[4-(meth)acryloyloxy]phenylethane-1-one represented by the following formula (A): (wherein R1 and R2, which may be identical to or different from each other, each represent a hydrogen atom

Synthesis and evaluation of quinoxaline derivatives as potential influenza NS1A protein inhibitors

A library of quinoxaline derivatives were prepared to target non-structural protein 1 of influenza A (NS1A) as a means to develop anti-influenza drug leads. An in vitro fluorescence polarization assay demonstrated that these compounds disrupted the dsRNA-NS1A interaction to varying extents. Changes of substituent at positions 2, 3 and 6 on the quinoxaline ring led to variance in responses. The most active compounds (35 and 44) had IC50 values in the range of low micromolar concentration without exhibiting significant dsRNA intercalation. Compound 44 was able to inhibit influenza A/Udorn/72 virus growth.