162407-08-1

Basic information

• Product Name: 1,4-Diazaspiro[4.5]deca-1,3-diene, 2,3-bis(4-methoxyphenyl)-
• CAS NO: 162407-08-1
• Molecular Formula: C22H24N2O2
• Molecular Weight: 348.445
• Mol File: 162407-08-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1,4-Diazaspiro[4.5]deca-1,3-diene, 2,3-bis(4-methoxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-Diazaspiro[4.5]deca-1,3-diene, 2,3-bis(4-methoxyphenyl)-(162407-08-1)
• EPA Substance Registry System: 1,4-Diazaspiro[4.5]deca-1,3-diene, 2,3-bis(4-methoxyphenyl)-(162407-08-1)

Safety Data

• Hazardous Substances Data: 162407-08-1(Hazardous Substances Data)

Upstream product

• 123-11-5 4-methoxy-benzaldehyde 
• 4464-76-0 1,2-bis(4-methoxyphenyl)-1,2-ethanediol 
• 108-94-1 cyclohexanone 
• 1226-42-2 1,2-bis(4-methoxyphenyl)-1,2-ethanedione 

Downstream Products

• 117106-36-2 d,l-1,2-diamino-1,2-bis(4-methoxyphenyl)ethane 

Relevant articles and documents

Convenient Routes to Symmetrical Benzils and Chiral 1,2-Diaryl-1,2-diaminoethanes, Useful Controllers and Probes for Enantioselective Synthesis

Pathways for the diastereoselective preparation of chiral 1,2-diaryl-1,2-diaminoethanes from ArCOOH, ArCHO or ArBr are described.

SULPHONYLATED DIPHENYLETHYLENEDIAMINES, METHOD FOR THEIR PREPARATION AND USE IN TRANSFER HYDROGENATION CATALYSIS

A diamine of formula (I) is described, in which A is hydrogen or a saturated or unsaturated C1-C20 alkyl group or an aryl group; B is a substituted or unsubstituted C1-C20 alkyl, cycloalkyl, alkaryl, alkaryl or aryl group or an alkylamino group and at least one of X1, X2, Y1, Y2 or Z is a C1-C10 alkyl, cycloalkyl, alkaryl, aralkyl or alkoxy substituting group. The chiral diamine may be used to prepare catalysts suitable for use in transfer hydrogenation reactions.