58479-52-0

Basic information

• Product Name: N-n-propylnorapomorphine
• Synonyms: N-n-propylnorapomorphine
• CAS NO: 58479-52-0
• Molecular Formula: C19H21NO2
• Molecular Weight: 295.37554
• Mol File: 58479-52-0.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 514°C at 760 mmHg
• Flash Point: 264.7°C
• Appearance: /
• Vapor Pressure: 3.46E-11mmHg at 25°C
• CAS DataBase Reference: N-n-propylnorapomorphine(CAS DataBase Reference)
• NIST Chemistry Reference: N-n-propylnorapomorphine(58479-52-0)
• EPA Substance Registry System: N-n-propylnorapomorphine(58479-52-0)

Safety Data

• Hazardous Substances Data: 58479-52-0(Hazardous Substances Data)

Usage

InChI:InChI=1/C19H21NO2.ClH/c1-2-9-20-10-8-12-4-3-5-14-17(12)15(20)11-13-6-7-16(21)19(22)18(13)14;/h3-7,15,21-22H,2,8-11H2,1H3;1H/t15-;/m0./s1

Upstream product

• 84579-79-3 (S)-(+)-10,11-dimethoxy-N-n-propylnorapomorphine hydrochloride 
• 1216940-66-7 norapomorphine mesylate 
• 107-08-4 1-iodo-propane 
• 81264-57-5 (R)-MDO-NPA 
• 50370-80-4 (+/-)-10,11-dimethoxy-N-n-propylnorapomorphine 

Downstream Products

• 81264-57-5 (R)-MDO-NPA 

Relevant articles and documents

One-pot N-dealkylation and acid-catalyzed rearrangement of morphinans into aporphines

The one-pot N-demethylation and acid-catalyzed rearrangement of morphinan-N-oxides offers a new, shorter and more efficient route to neuropharmacologically important N-substituted aporphines. An improved procedure is described for the preparation of the starting alkaloid N-oxides using Na2WO4 as catalyst. The transetherification during the rearrangement of codeinone into 2-O-alkyl-norapocodeines is documented.

Aporphines. 35. Synthesis of (R)-(-)- and (S)-(+)-Apomorphine from Thebaine and (+)-Bulbocapnine

A practical method for the synthesis of (-)-apomorphine and (-)-N-n-propylnorapomorphine from the opioid thebaine is presented.The method is also applicable to the transformation of (+)-bulbocapnine to (+)-apomorphine.