73174-99-9

Basic information

• Product Name: 13-cis-retinoyl chloride
• Synonyms: 13-cis-retinoyl chloride
• CAS NO: 73174-99-9
• Molecular Weight: 318.887
• Mol File: 73174-99-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 13-cis-retinoyl chloride(CAS DataBase Reference)
• NIST Chemistry Reference: 13-cis-retinoyl chloride(73174-99-9)
• EPA Substance Registry System: 13-cis-retinoyl chloride(73174-99-9)

Safety Data

• Hazardous Substances Data: 73174-99-9(Hazardous Substances Data)

Upstream product

• 4759-48-2 13-cis-retinoic acid 

Downstream Products

• 110769-95-4 N-(13-cis-retinoyl)-L-alanine ethyl ester 
• 110769-91-0 N-(13-cis-retinoyl)-L-leucine ethyl ester 
• 110770-00-8 N-(13-cis-retinoyl)-DL-phenylalanine methyl ester 
• 110770-01-9 N-(13-cis-retinoyl)-DL-phenylalanine 
• 110769-94-3 N-(13-cis-retinoyl)-L-phenylalanine 
• 110769-92-1 N-(13-cis-retinoyl)-L-leucine 
• 110770-02-0 N-(13-cis-retinoyl)-DL-alanine 
• 110769-96-5 N-(13-cis-retinoyl)-L-alanine 
• 110848-62-9 N-(13-cis-retinoyl)glycine 
• 84680-30-8 13-cis-N-Butylretinamide 
• 75686-07-6 (2Z,4E,6E,8E)-N-(4-hydroxyphenyl)-3,7-dimethyl-9-(2,6,6-trimethylcyclohex-1-en-1-yl)nona-2,4,6,8-tetraenamide 
• 110848-61-8 N-(13-cis-retinoyl)glycine ethyl ester 
• 138752-01-9 13-(Z)-retinoic anhydride 
• 75686-04-3 13-cis-N-Ethylretinamide 

Relevant articles and documents

SYNTHETIC INVESTIGATIONS IN THE CHEMISTRY OF POLYENE COMPOUNDS LI. SYNTHESIS OF THE ANHYDRIDES OF ISOMERIC RETINOIC ACIDS

A series of anhydrides of isomeric retinoic acids, which are biologically active retinoids, were synthesized.It was shown that three alternative methods can be used for the synthesis of the symmetrical anhydride of all-(E)-retinoic acid.Decomposition of t

Synthesis and properties of some 13-cis- and all-trans-retinamides

Several 13-cis-retinamides were synthesized from 13-cis-retinoic acid via either 13-cis-retinoyl chloride or 13-cis-1-retinoylimidazole. All-trans-retinoylglycine was prepared from all-trans-retinoyl chloride and ethyl glycinate. Detailed procedures were developed for the preparation of other all-trans-retinamides on a large scale for studies of the chemoprevention of cancer.