65725-89-5

Basic information

• Product Name: Benzene, 1-methoxy-4-(2-methoxypropyl)-
• CAS NO: 65725-89-5
• Molecular Formula: C11H16O2
• Molecular Weight: 180.247
• Mol File: 65725-89-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzene, 1-methoxy-4-(2-methoxypropyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-methoxy-4-(2-methoxypropyl)-(65725-89-5)
• EPA Substance Registry System: Benzene, 1-methoxy-4-(2-methoxypropyl)-(65725-89-5)

Safety Data

• Hazardous Substances Data: 65725-89-5(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 1232133-20-8 1-(4-methoxyphenyl)propan-2-yl 2-phenylbenzoate 
• 4180-23-8 E-1-(4'-methoxyphenyl)prop-1-ene 
• 133586-93-3 4-Nitro-benzenesulfonic acid 2-(4-methoxy-phenyl)-1-methyl-ethyl ester 
• 134906-48-2 4-Chloro-benzenesulfonic acid 2-(4-methoxy-phenyl)-1-methyl-ethyl ester 
• 134906-47-1 Benzenesulfonic acid 2-(4-methoxy-phenyl)-1-methyl-ethyl ester 
• 898-95-3 1-(4-methoxy-phenyl)-2-(toluene-4-sulfonyloxy)-propane 

Downstream Products

• 123-11-5 4-methoxy-benzaldehyde 

Relevant articles and documents

Novel Oxidative Ugi Reaction for the Synthesis of Highly Active, Visible-Light, Imide-Acridinium Organophotocatalysts

A newly designed class of acridinium-based organophotocatalysts bearing an imide group at the C9-position is presented. To achieve these unprecedented structures, a synthetic strategy based on a novel straightforward oxidative Ugi-type reaction at the benzylic position of C9-unsubstituted acridanes was developed. The introduction of the imide-unit affords a notable photocatalytic activity enhancement, allowing efficient transformations in different oxidative and reductive visible-light catalytic reactions.

Addition reaction of 2-phenylbenzoic acid onto unactivated olefins catalyzed by Ru(II)-xantphos catalysis

Ru(II)-xantphos catalysis is found to be effective for the addition reaction of 2-phenylbenzoic acid onto unactivated olefins. Thus, the reactions of 2-phenylbenzoic acid and unactivated olefins are carried out in the presence of 5 mol % of Ru(II)-xantpho