23876-59-7

Basic information

• Product Name: 2-Methyl-1H-indol-3-ylaMine
• Synonyms: 2-Methyl-1H-indol-3-ylaMine
• CAS NO: 23876-59-7
• Molecular Formula: C₉H₁₀N₂
• Molecular Weight: 146.1891
• Mol File: 23876-59-7.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-Methyl-1H-indol-3-ylaMine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Methyl-1H-indol-3-ylaMine(23876-59-7)
• EPA Substance Registry System: 2-Methyl-1H-indol-3-ylaMine(23876-59-7)

Safety Data

• Hazardous Substances Data: 23876-59-7(Hazardous Substances Data)

Upstream product

• 7647-01-0 hydrogenchloride 
• 35261-42-8 2-(2-methyl-1H-indol-3-yl)isoindole-1,3-dione 

Downstream Products

• 6872-06-6 2-methyl indoline 
• 655250-38-7 2-(p-dimethylaminophenylmethyleneimino)aminoacetylmethyl-3-(2'-methyl-indol-3'-yl)-6-bromo-4(3H)-quinazolinone 
• 655250-39-8 2-(o-chlorophenylmethyleneimino)aminoacetylmethyl-3-(2'-methyl-indol-3'-yl)-6-bromo-4(3H)-quinazolinone 
• 655250-33-2 2-(o-methoxyphenylmethyleneimino)aminoacetylmethyl-3-(2'-methylindol-3'-yl)-4(3H)-quinazolinone 
• 655250-32-1 2-(p-methoxyphenylmethyleneimino)aminoacetylmethyl-3-(2'-methylindol-3'-yl)-4(3H)-quinazolinone 
• 655250-31-0 2-(o-methoxyphenylmethyleneimino)aminoacetylmethyl-3-(2'-methylindol-3'-yl)-4(3H)-quinazolinone 

Relevant articles and documents

Azolyacetones as precursors to indoles and naphthofurans facilitated by microwave irradiation with simultaneous cooling

Phthalimide reacted with phenacyl bromide under microwave irradiation to yield phenacyl isoindolidene-1,3-dione (3b), while 3a reacted with phenylhydrazine to yield the phenylhydrazone 4 that was readily converted into indoylphthalimide 8. Similarly N-benzotriazolylacetone (6a) reacted with phenyl hydrazine to yield the phenylhydrazone 7a that was converted into indoylbenzotriazole 9. Treatment of 8 with hydrazine hydrate afforded a mixture of phthalhydrazide 10 and 3-amino-2-methylindole (11). Reacting enaminone 13 with naphthoquinone (14) afforded the aryl naphthofuran 17. The possibility of the formation of the aldehyde 18 was excluded based on HMQC, which revealed that the carbonyl carbon is not linked to any hydrogen.