804553-24-0

Basic information

• Product Name: Benzaldehyde, 2-(3-oxobutyl)-
• CAS NO: 804553-24-0
• Molecular Formula: C11H12O2
• Molecular Weight: 176.215
• Mol File: 804553-24-0.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzaldehyde, 2-(3-oxobutyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzaldehyde, 2-(3-oxobutyl)-(804553-24-0)
• EPA Substance Registry System: Benzaldehyde, 2-(3-oxobutyl)-(804553-24-0)

Safety Data

• Hazardous Substances Data: 804553-24-0(Hazardous Substances Data)

Upstream product

• 1574475-07-2 C₁₄H₂₁NO₄ 
• 643-79-8 o-phthalic dicarboxaldehyde 
• 1574475-06-1 C₁₄H₂₀O₄ 
• 86867-62-1 (E)-3-(2-formylphenyl)propenoic acid ethyl ester 
• 598-32-3 2-hydroxy-3-butene 
• 6630-33-7 ortho-bromobenzaldehyde 
• 2717-44-4 2-methyl-3,4-dihydronaphthalene 

Downstream Products

• 1574474-98-8 C₁₅H₂₁NO₂S 

Relevant articles and documents

Asymmetric synthesis of novel vicinal amino alcohols via intramolecular ketone- N -sulfinylimine pinacol-type reductive coupling promoted by SmI 2

A novel intramolecular asymmetric ketone-N-sulfinylimine pinacol-type reductive coupling reaction induced by SmI2 was reported. A series of 1-amino-1,2,3,4-tetrahydronaphthalen-2-carbinols were obtained in moderate to good yields with excellent

Thiazolium ylide-catalyzed intramolecular aldehyde-ketone benzoin-forming reactions: Substrate scope

The scope and limitations of intramolecular benzoin-forming reactions of aldehydes and ketones catalyzed by the combination of a thiazolium salt and a base are described. After optimization of the reaction conditions, five- and six-membered cyclic acyloins were obtained in good to excellent yields and competing reactions such as intramolecular aldol reactions were suppressed. The analogous closure of seven-membered rings proved difficult.