53654-36-7

Basic information

• Product Name: 1H-Indole, 3-ethenyl-
• Synonyms: 3-Vinyl-indol;YAMMUQMONCMYCX-UHFFFAOYSA;3-vinyl-1H-indole;1H-Indole,3-ethenyl;InChI=1/C10H9N/c1-2-8-7-11-10-6-4-3-5-9(8)10/h2-7,11H,1H2;3-vinyl-indole
• CAS NO: 53654-36-7
• Molecular Formula: C10H9N
• Molecular Weight: 143.188
• Mol File: 53654-36-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1H-Indole, 3-ethenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Indole, 3-ethenyl-(53654-36-7)
• EPA Substance Registry System: 1H-Indole, 3-ethenyl-(53654-36-7)

Safety Data

• Hazardous Substances Data: 53654-36-7(Hazardous Substances Data)

Usage

Structure

Benzene ring fused to a pyrrole ring

Classification

Essential amino acid

Role

Important for the production of serotonin, melatonin, and protein synthesis

Effects

Contributes to mood regulation, sleep, and appetite

Dietary sources

Turkey, chicken, and dairy products

Availability

Dietary supplement for mood-boosting and sleep-improving effects.

Upstream product

• 10604-59-8 N-Ethylindole 

Downstream Products

• 1318151-79-9 (1S,2S,9aR)-tert-butyl 2'-oxo-2-phenyl-2,3,9,9a-tetrahydrospiro[carbazole-1,3'-indoline]-1'-carboxylate 
• 1318152-05-4 C₃₀H₂₈N₂O₃ 
• 1318151-69-7 (1S,2S,9aR)-tert-butyl 2-benzoyl-2'-oxo-2,3,9,9a-tetrahydrospiro[carbazole-1,3'-indoline]-1'-carboxylate 
• 1318151-97-1 C₃₁H₂₈N₂O₄ 
• 1318151-67-5 (1S,2S,9aR)-2-benzyl 1'-tert-butyl 2'-oxo-2,3,9,9a-tetrahydrospiro[carbazole-1,3'-indoline]-1',2-dicarboxylate 
• 1318151-94-8 C₃₂H₃₀N₂O₅ 
• 1318151-72-2 (1S,2S,9aR)-tert-butyl 2-(4-chloro-benzoyl)-2'-oxo-2,3,9,9a-tetrahydrospiro[carbazole-1,3'-indoline]-1'-carboxylate 
• 1318152-00-9 C₃₁H₂₇ClN₂O₄ 
• 1318151-77-7 (1S,2S,9aR)-tert-butyl 2'-oxo-2-tosyl-2,3,9,9a-tetrahydrospiro[carbazole-1,3'-indoline]-1'-carboxylate 
• 1318152-03-2 C₃₁H₃₀N₂O₅S 

Relevant articles and documents

CATALYTIC SYNTHESIS OF 1-VINYLINDOLE

A new method is proposed for the synthesis of 1-vinylindole by catalytic dehydrogenation of 1-ethylindole.The dehydrogenation of 1-ethylindole is accompanied by its isomerization to 3-ethylindole.