61319-45-7

Basic information

• Product Name: N-(all-trans-Retinoyl)-imidazole
• Synonyms: N-(all-trans-Retinoyl)-imidazole
• CAS NO: 61319-45-7
• Molecular Weight: 350.504
• Mol File: 61319-45-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N-(all-trans-Retinoyl)-imidazole(CAS DataBase Reference)
• NIST Chemistry Reference: N-(all-trans-Retinoyl)-imidazole(61319-45-7)
• EPA Substance Registry System: N-(all-trans-Retinoyl)-imidazole(61319-45-7)

Safety Data

• Hazardous Substances Data: 61319-45-7(Hazardous Substances Data)

Upstream product

• 302-79-4 all-trans-retinoic-acid 
• 530-62-1 1,1'-carbonyldiimidazole 

Downstream Products

• 71869-12-0 all-trans retinoic acid-β-D-glucopyranosyl ester 
• 79787-62-5 1,2-dihydro-2,2,4-trimethyl-6-quinolinyl retinoate 
• 79787-61-4 (all-E)-1-[3,7-dimethyl-1-oxo-9-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2,4,6,8-nonatetraenyl]-6-ethoxy-1,2-dihydro-2,2,4-trimethylquinoline 
• 1290540-26-9 (3R,3'RS,6'R)-3-methoxy-β,ε-caroten-3'-retinoate 
• 1290540-13-4 (3R,3'R)-zeaxanthin monoretinoate 
• 1290540-14-5 (3R,3'R)-zeaxanthin diretinoate 
• 1290540-27-0 (2'R)-aleuriaxanthin retinoate 
• 1290540-18-9 (9Z,9'Z; 3R,3'R)-alloxanthin monoretinoate 
• 1290540-19-0 (9Z,9'Z; 3R,3'R)-alloxanthin diretinoate 
• 1290540-15-6 (3S,3'S)-zeaxanthin monoretinoate 
• 1290540-16-7 (3S,3'S)-zeaxanthin diretinoate 
• 1290540-20-3 (3R,3'R)-3,3'-dihydroxy-7,8,7',8'-tetrahydro-β,β-carotene-8,8'-dione monoretinoate 
• 1290540-21-4 (3R,3'R)-3,3'-dihydroxy-7,8,7',8'-tetrahydro-β,β-carotene-8,8'-dione diretinoate 
• 34026-74-9 astacene 

Relevant articles and documents

27. Carotinoid-Glycosylester. Synthese von 8'-Apo-β-carotin-8'-saure-(β-D-glucosyl)ester und Vitamin-A-saure-(β-D-glucosyl)ester

β-D-glucosyl 8'-apo-β-carotene-8'-oate (III) and β-D-glucosyl vitamin-A-oate (VI) were regio- and stereoselctively synthesized in high yields from the N-acyl-imidazoles I and IV, respectively, or from the N-acyltriazoles II and V, resprctively, and unprotected β-D-glucose, according to the method described for the synthesis of di(β-D-glucosyl) 8,8'-diapo-carotene8,8'-dioate .It seems that this method can generally be applied for the synthesis of β-D-glucosyl esters of polyene carboxylic acids.

Novel retinoic acid metabolism blocking agents endowed with multiple biological activities are efficient growth inhibitors of human breast and prostate cancer cells in vitro and a human breast tumor xenograft in nude mice

Novel retinoic acid metabolism blocking agents (RAMBAs) have been synthesized and characterized. The synthetic features include introduction of nucleophilic ligands at C-4 of all-trans-retinoic acid (ATRA) and 13-cis-retinoic acid, and modification of ter