21997-97-7

Basic information

• Product Name: 3-(3,4-dimethoxy-phenyl)-propionyl azide
• Synonyms: 3-(3,4-dimethoxy-phenyl)-propionyl azide
• CAS NO: 21997-97-7
• Molecular Weight: 235.243
• Mol File: 21997-97-7.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 3-(3,4-dimethoxy-phenyl)-propionyl azide(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(3,4-dimethoxy-phenyl)-propionyl azide(21997-97-7)
• EPA Substance Registry System: 3-(3,4-dimethoxy-phenyl)-propionyl azide(21997-97-7)

Safety Data

• Hazardous Substances Data: 21997-97-7(Hazardous Substances Data)

Upstream product

• 5462-13-5 ethyl 3-(3,4-dimethoxyphenyl)propionate 
• 27798-73-8 methyl 3-(3,4-dimethoxyphenyl)propionate 
• 2107-70-2 3,4-methoxycinnamic acid 
• 88368-71-2 3-(3,4-dimethoxyphenyl)propionic acid hydrazide 
• 51842-87-6 3-(3,4-dimethoxy-phenyl)-propionyl chloride 

Downstream Products

• 104058-26-6 1-Allyl-1-benzyl-3-[2-(3,4-dimethoxy-phenyl)-ethyl]-urea 
• 104058-22-2 [2-(3,4-Dimethoxy-phenyl)-ethyl]-carbamic acid 1-methyl-allyl ester 
• 88387-98-8 [2-(3,4-Dimethoxy-phenyl)-ethylcarbamoyloxy]-acetic acid ethyl ester 
• 446853-44-7 N-(3,4-dimethoxy-phenethyl)-N'-p-tolyl-urea 
• 700855-80-7 N-(3,4-dimethoxy-phenethyl)-N'-m-tolyl-urea 
• 67616-08-4 N'-phenyl-N-<2-(3,4-dimethoxyphenyl)ethyl>urea 
• 859195-16-7 (6,7-dimethoxy-3,4-dihydro-[1]isoquinolyl)-methyl-phenyl-amine 
• 39052-28-3 (6,7-dimethoxy-3,4-dihydro-2H-[1]isochinolyLiDene)-m-tolyl-amine 
• 39052-30-7 (6,7-dimethoxy-3,4-dihydro-2H-[1]isochinolyLiDene)-p-tolyl-amine 
• 39052-32-9 6,7-Dimethoxy-1-[(E)-phenylimino]-1,2,3,4-tetrahydroisochinolin 
• 25017-47-4 N-<2-(3,4-dimethoxyphenylethyl)>urea 
• 493-49-2 6,7-dimethoxy-3,4-dihydro-2H-isoquinolin-1-one 
• 486-99-7 (6,7-dimethoxy-1,2,3,4-tetrahydro-1-isoquinolyl)methanol 
• 93598-34-6 (+/-)-N-methylcalycotomine 

Relevant articles and documents

Efficient synthesis of tetrahydro-b-carbolin-1-one and dihydroisoquinolin- 1-one derivatives as versatile Intermediates

An efficient one-pot procedure is described in which an isocyanate intermediate, generated from the corresponding carboxylic acid by a modified Curtius rearrangement, is captured by a tethered aromatic ring in the presence of BF3?OEt2 to generate various

AN ENANTIOSELECTIVE SYNTHESIS OF 1-(α-HYDROXYALKYL)-1,2,3,4-TETRAHYDROISOQUINOLINES THROUGH OPTICALLY ACTIVE N-OXAACYLIMINIUM ION INTERMEDIATES

An enantioselective synthesis of 1S-(1'S-hydroxyethyl)- 1S-(1'S-hydroxybenzyl)- and 1R-(1'R-hydroxybenzyl)-1,2,3,4-tetrahydroisoquinoline was achieved by reductive cleavage of the oxazolidinone ring of the correspponding 1-substituted oxazoloisoqui

A cyclization of β-arylethylisocyanates to 3,4-dihydroisocarbostyrils

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