95033-78-6

Basic information

• Product Name: 1H-2-Benzopyran-1-ol, 3,4-dihydro-
• CAS NO: 95033-78-6
• Molecular Formula: C9H10O2
• Molecular Weight: 150.177
• Mol File: 95033-78-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1H-2-Benzopyran-1-ol, 3,4-dihydro-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-2-Benzopyran-1-ol, 3,4-dihydro-(95033-78-6)
• EPA Substance Registry System: 1H-2-Benzopyran-1-ol, 3,4-dihydro-(95033-78-6)

Safety Data

• Hazardous Substances Data: 95033-78-6(Hazardous Substances Data)

Usage

Derivative of

Coumarin

Usage

Different sources of media describe the Usage of 95033-78-6 differently. You can refer to the following data:
1. Flavoring agent in food products
2. Fragrance in perfumes and cosmetics

Aroma

Sweet, vanilla-like

Natural occurrence

Found in some plants

Studied properties

Different sources of media describe the Studied properties of 95033-78-6 differently. You can refer to the following data:
1. Anticoagulant
2. Anti-inflammatory

Potential therapeutic applications

Different sources of media describe the Potential therapeutic applications of 95033-78-6 differently. You can refer to the following data:
1. Diabetes treatment
2. Alzheimer's disease treatment

Consumption warning

Excessive consumption or exposure can be harmful

Allergen status

Identified as a potential allergen

Upstream product

• 493-05-0 isochromane 
• 124-41-4 sodium methylate 
• 125593-23-9 2-(2-hydroxyethyl)benzaldehyde tosylhydrazone 
• 4702-34-5 isochroman-1-one 

Downstream Products

• 95033-79-7 2-<2-(Hydroxyethyl)phenyl>indan-1,3-dione 
• 75802-18-5 2-(β-hydroxyethyl)benzaldehyde 
• 125593-22-8 2-(2-Hydroxy-ethyl)-benzaldehyde oxime 
• 324027-23-8 2-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-benzaldehyde 
• 100008-34-2 2-(2,4-dihydro-1H-isochromen-1-yl)-1-phenylethanone 
• 4702-34-5 isochroman-1-one 
• 13328-80-8 1-Cyan-isochroman 
• 950502-65-5 [2-(2-fluoro-phenyl)-ethyl]-[2-(2-hydroxy-ethyl)-benzyl]-carbamic acid tert-butyl ester 
• 82746-16-5 (3,4-dihydro-1H-2-benzopyran-1-yl)-4-N-toluenesulfonamide 
• 2292-59-3 3,4-Dihydro-1-phenyl-1H-benzopyran 
• 35050-30-7 2-(2-hydroxyethyl)benzylamine hydrochloride 
• 125593-24-0 <2-(2-hydroxyethyl)phenyl>diazomethane 
• 125593-33-1 2-ethoxymethyl-phenethyl alcohol 
• 125593-32-0 2-(2-methoxymethylphenyl)ethanol 

Relevant articles and documents

Catalytic enantioselective oxidative cross-coupling of benzylic ethers with aldehydes

The first one-pot enantioselective oxidative coupling of cyclic benzylic ethers with aldehydes has been developed. A variety of benzylic ethers were transformed into the corresponding oxygen heterocycles with high enantioselectivity. Mechanistic experiments were conducted to determine the nature of the reaction intermediates. The application of this strategy to coupling reactions with other nucleophiles besides aldehydes was also explored. In one go: The first one-pot enantioselective oxidative coupling of cyclic benzylic ethers with aldehydes has been developed. A variety of benzylic ethers could be functionalized with this method, and the corresponding oxygen heterocycles were obtained with high enantioselectivity.

Cobalt-Catalyzed Partial Oxidation of Olefins and Ethers Using Molecular Oxygen

Co(acac)3 catalyzes the aerobic oxidation of vinyl aromatic compounds ArCH=CH2 with formation of ArCO2H and ArCHO, and also the aerobic oxidation of cyclic ethers with formation of the corresponding lactones.