1746-89-0

Basic information

• Product Name: 2-ALLYLBENZENE-1,3-DIOL
• Synonyms: 2-ALLYLBENZENE-1,3-DIOL;2-ALLYLRESORCINOL;1,3-Benzenediol, 2-(2-propen-1-yl)-
• CAS NO: 1746-89-0
• Molecular Formula: C₉H₁₀O₂
• Molecular Weight: 150.17
• Product Categories: Miscellaneous
• Mol File: 1746-89-0.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-ALLYLBENZENE-1,3-DIOL(CAS DataBase Reference)
• NIST Chemistry Reference: 2-ALLYLBENZENE-1,3-DIOL(1746-89-0)
• EPA Substance Registry System: 2-ALLYLBENZENE-1,3-DIOL(1746-89-0)

Safety Data

• Hazardous Substances Data: 1746-89-0(Hazardous Substances Data)

Usage

Physical State

Colorless, viscous liquid

Odor

Sweet, floral

Uses

Manufacturing of fragrances and flavors
Pharmaceuticals
Chemical intermediate in organic synthesis
Antioxidant and anti-inflammatory properties
Production of dyes
Stabilizer for rubber and plastics

Upstream product

• 1616-54-2 8-allyl-7-hydroxy-4-methylcoumarin 
• 623-11-0 1-methyl-4-nitrosobenzene 
• 3993-57-5 7-allyloxy-4-methyl-2H-chromen-2-one 
• 1616-51-9 3-allyloxyphenol 
• 91-66-7 N,N-diethylaniline 
• 939017-92-2 2-allyl-1,3-bis(methoxymethoxy)benzene 
• 107-18-6 allyl alcohol 
• 108-46-3 recorcinol 
• 57234-29-4 1,3-bis(methoxymethyl)resorcinol 
• 90-33-5 7-hydroxy-4-methyl-chromen-2-one 

Downstream Products

• 13331-19-6 2-propyl-1,3-benzenediol 
• 3698-35-9 1,3-dimethoxy-2-(2-propenyl)benzene 
• 939017-93-3 2-allyl-1,3-bis(tert-butyldimethylsilyloxy)benzene 
• 939017-94-4 2-(2,6-bis(tert-butyldimethylsilyloxy)phenyl)acetaldehyde 
• 939017-95-5 ethyl (E)-4-(2,6-bis(tert-butyldimethylsilyloxy)phenyl)-2-methylbut-2-enoate 
• 939017-96-6 (E)-4-(2,6-bis(tert-butyldimethylsilyloxy)phenyl)-2-methylbut-2-en-1-ol 
• 939017-97-7 (E)-4-(2,6-bis(tert-butyldimethylsilyloxy)phenyl)-2-methylbut-2-enyl methyl carbonate 
• 939017-98-8 (E)-4-(2,6-dihydroxyphenyl)-2-methylbut-2-enyl methyl carbonate 
• 700-44-7 6-methoxysalicylaldehyde 
• 40786-69-4 1-(2,4-dihydroxy-3-propylphenyl)ethanone 
• 387-46-2 2,6-dihydroxybenzaldehyde 
• 114568-18-2 (E)-1,3-dimethoxy-2-(prop-1-en-1-yl)benzene 
• 3392-97-0 2,6-dimethoxybenzaldehyde 
• 1609641-39-5 2,4,6-tris[(1E)-prop-1-en-1-yl]benzene-1,3-diol 

Relevant articles and documents

Structure–activity relationships and docking studies of hydroxychavicol and its analogs as xanthine oxidase inhibitors

Hydroxychavicol (HC), which is obtained from the leaves of Piper betle LINN. (Piperaceae), inhibits xanthine oxidase (XO) with an IC50 value of 16.7μM, making it more potent than the clinically used allopurinol (IC50=30.7μM). Herein, a structure–activity relationship analysis of the polar part analogs of HC was conducted and an inhibitor was discovered with a potency 13 times that of HC. Kinetic studies have revealed that HC and its active analog inhibit XO in an uncompetitive manner. The binding structure prediction of these inhibitor molecules to the XO complex with xanthine suggested that both compounds (HC and its analog) could simultaneously form hydrogen bonds with xanthine and XO.

Stereoselective syntheses of the 2-isopropenyl-2,3-dihydrobenzofuran nucleus: Potential chiral building blocks for the syntheses of tremetone, hydroxytremetone, and rotenone

(Chemical Equation Presented) The first enantioselective synthesis of the 2-isopropenyl-2,3-dihydrobenzofuran skeleton of tremetone and hydroxytremetone from (E)-4-(2-hydroxyphenyl)-2-methyl-2-butenyl methyl carbonate and (E)-4-(2,6-dihydroxyphenyl)-2-met

Regioselectivity in aromatic Claisen rearrangements

Theoretical calculations and the isomeric product composition for a series of eight meta-substituted allyl aryl ethers confirm the reliability of a new 1H NMR methodology used to predict aromatic Claisen regioselectivity from ground-state confo