65610-01-7

Basic information

• Product Name: meso-3,4-diphenyl-adipic acid
• Synonyms: meso-3,4-diphenyl-adipic acid
• CAS NO: 65610-01-7
• Molecular Weight: 298.339
• Mol File: 65610-01-7.mol

Chemical Properties

• CAS DataBase Reference: meso-3,4-diphenyl-adipic acid(CAS DataBase Reference)
• NIST Chemistry Reference: meso-3,4-diphenyl-adipic acid(65610-01-7)
• EPA Substance Registry System: meso-3,4-diphenyl-adipic acid(65610-01-7)

Safety Data

• Hazardous Substances Data: 65610-01-7(Hazardous Substances Data)

Upstream product

• 19799-42-9 3,4-bis(phenyl)thiophene-2,5-dicarboxylic acid 
• 110195-60-3 3,4-diphenyl-hexene-(3c)-dioic acid 
• 119-61-9 benzophenone 
• 501-52-0 3-Phenylpropionic acid 
• 17377-82-1 (E)-1-methylpropyl cinnamate 
• 71-43-2 benzene 
• 110195-60-3 3,4-diphenyl-hexene-(3t)-dioic acid 
• 103-26-4 Methyl cinnamate 
• 25347-44-8 racem.-3,4-diphenyl-adipic acid 
• 623-11-0 1-methyl-4-nitrosobenzene 
• 7028-47-9 dimethyl (3SR,4SR)-3,4-diphenylhexanedioate 
• 140-10-3 (E)-3-phenylacrylic acid 
• 100-42-5 styrene 
• 142560-16-5 tetramethyl dl-2,3-diphenylbutane-1,1,4,4-tetracarboxylate 

Downstream Products

• 108305-59-5 meso-3,4-diphenyl-adipic acid-dichloride 
• 1772-53-8 meso-3,4-bis-(4-chloro-phenyl)-adipic acid 
• 64-19-7 acetic acid 
• 65-85-0 benzoic acid 
• 25347-44-8 3,4-diphenyl-adipic acid 
• 108305-59-5 racem.-3,4-diphenyl-adipic acid-dichloride 
• 1772-53-8 d,l-3,4-Bis-<4-chlorphenyl>-adipinsaeure 
• 7028-47-9 dimethyl (3SR,4SR)-3,4-diphenylhexanedioate 
• 94546-11-9 racem.-3,4-bis-(4-nitro-phenyl)-adipic acid dimethyl ester 
• 38462-80-5 (+/-)-phenyl-(2,4r,5t-triphenyl-cyclopent-1-enyl)-ketone 
• 38462-79-2 (+/-)-phenyl-(2,4c,5t-triphenyl-cyclopent-2-en-r-yl)-ketone 
• 94546-11-9 meso-3,4-bis-(4-nitro-phenyl)-adipic acid dimethyl ester 
• 77053-39-5 meso-3,4-bis-(4-hydroxy-phenyl)-adipic acid 
• 61883-07-6 meso-3,4-diphenyl-adipic acid dimethyl ester 

Relevant articles and documents

Stereoselective hydrocoupling of cinnamic acid esters by electroreduction: Application to asymmetric synthesis of hydrodimers

The electroreduction of Ar-substituted methyl cinnamates in acetonitrile gave all-trans cyclized hydrodimers stereoselectively (58-90% de). In all cases, small amounts (2-symmetric dl-3,4-diaryladipic acids and trans-3,4-diarylcyclopentanones. The chiral auxiliary [(1R)-exo]-3-exo-(diphenylmethyl)borneol, prepared from (1R)-(+)-camphor, was highly effective for the stereoselective hydrocoupling of its cinnamates by electroreduction. From the resulting hydrodimers, (3R,4R)-3,4-diaryladipic acid esters and (3R,4R)-3,4-diarylhexane-1,6-diols were synthesized in 87-95% ee.