754215-63-9

Basic information

• Product Name: 1,3,5-Benzenetriol, 2-(phenylmethyl)- (9CI)
• Synonyms: 1,3,5-Benzenetriol, 2-(phenylmethyl)- (9CI)
• CAS NO: 754215-63-9
• Molecular Formula: C13H12O3
• Molecular Weight: 216.23258
• Product Categories: ALCOHOL
• Mol File: 754215-63-9.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,3,5-Benzenetriol, 2-(phenylmethyl)- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,5-Benzenetriol, 2-(phenylmethyl)- (9CI)(754215-63-9)
• EPA Substance Registry System: 1,3,5-Benzenetriol, 2-(phenylmethyl)- (9CI)(754215-63-9)

Safety Data

• Hazardous Substances Data: 754215-63-9(Hazardous Substances Data)

Usage

Derivative of

Benzenetriol

Contains

A phenylmethyl group attached to the benzene ring

Field of use

Organic chemistry

Reactivity

Unique reactivity

Application

Building block for the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds

Antioxidant properties

Yes

Skincare and cosmetic use

Protects against oxidative stress and free radical damage

Upstream product

• 3555-86-0 2-benzoylphloroglucinol 
• 108-73-6 3,5-dihydroxyphenol 
• 100-39-0 benzyl bromide 
• 100-52-7 benzaldehyde 
• 100-47-0 benzonitrile 
• 100-44-7 benzyl chloride 

Relevant articles and documents

Carbon glycoside compound as well as preparation and application thereof

The invention discloses a carbon glycoside compound as well as preparation and application thereof, and particularly relates to a carbon glycoside compound as shown in a general formula (I), a preparation method of the carbon glycoside compound, and application of a pharmaceutical composition containing the compound in inhibiting sodium-dependent glucose transporter 2, SGLT-2 and the application in preparation of drugs for treating and preventing diabetes and complications.

Divergent synthesis of hydrophilic dendrons based on tri(ethylene glycol) spacers

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Hydrogenation of substituted aromatic aldehydes: Nucleophilic trapping of the reaction intermediate, application to the efficient synthesis of methylene linked flavanol dimers

The synthesis of dimeric flavanols is the consequence of the possible trapping of the reaction intermediates generated in the course of the reductive hydrogenation of substituted benzaldehydes. The scope of this reaction is investigated.