81868-12-4

Basic information

• Product Name: 5-BROMOTRYPTAMINE HYDROCHLORIDE
• Synonyms: 5-BROMOTRYPTAMINE HYDROCHLORIDE;3-(2-AMINOETHYL)-5-BROMOINDOLE HCL;3-(2-AMINOETHYL)-5-BROMOINDOLE HYDROCHLORIDE;5-BromotryptamineHCl;5-Bromotryptaminehydrochloride,98%;2-(5-bromo-1H-indol-3-yl)ethanamine hydrochloride;2-(5-BroMo-1H-indol-3-yl)-ethylaMine hydrochloride;2-(5-Bromo-1H-indol-3-yl)
• CAS NO: 81868-12-4
• Molecular Formula: C₁₀H₁₁BrN₂*ClH
• Molecular Weight: 275.57
• Product Categories: Tryptamines
• Mol File: 81868-12-4.mol
• Article Data: 1

Chemical Properties

• Melting Point: 274°C (dec.)
• Boiling Point: 419.9°C at 760 mmHg
• Flash Point: 207.7°C
• Appearance: /
• Vapor Pressure: 1.88E-07mmHg at 25°C
• Storage Temp.: Inert atmosphere,Room Temperature
• Sensitive: Light Sensitive
• BRN: 3728224
• CAS DataBase Reference: 5-BROMOTRYPTAMINE HYDROCHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 5-BROMOTRYPTAMINE HYDROCHLORIDE(81868-12-4)
• EPA Substance Registry System: 5-BROMOTRYPTAMINE HYDROCHLORIDE(81868-12-4)

Safety Data

• Hazard Codes: Xn
• Statements: 22-36/38
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 81868-12-4(Hazardous Substances Data)

Usage

Uses

5-Bromotryptamine hydrochloride is used as pharmaceutical intermediates.

InChI:InChI=1/C10H11BrN2.ClH/c11-8-1-2-10-9(5-8)7(3-4-12)6-13-10;/h1-2,5-6,13H,3-4,12H2;1H

Upstream product

• 3610-42-2 5-bromotryptamine 

Downstream Products

• 1382991-51-6 N-(2-(5-bromo-1H-indol-3-yl)ethyl)-4-(3-fluorobenzyl)benzamide 
• 486-84-0 harmane 
• 1366416-68-3 C₂₀H₂₁BrN₂ 
• 1366416-41-2 N-allyl-N-benzyl-(5-bromo)tryptamine 
• 79894-12-5 N-benzyl-(5-bromo)tryptamine 
• 17274-65-6 5-bromo-3-[2-(N,N-dimethylamino)ethyl]-1H-indole 
• 174021-63-7 tert-butyl N-[2-(5-bromo-1H-indol-3-yl)ethyl]carbamate 
• 853019-30-4 6-bromo-1'-(2-phenoxyethyl)-2,3,4,9-tetrahydrospiro[β-carboline-1,3'-pyrrolidine] 
• 1355043-47-8 dimethyl-9-bromo-3-(2-hydroxybenzoyl)-6,7,12,12b-tetrahydro-indolo[2,3-a]quinolizine-1,12b-dicarboxylate 

Relevant articles and documents

The crystalline forms of nine hydrochloride salts of substituted tryptamines

The crystal structures of the hydro chloride salts of nine substituted tryptamines, namely, 1-methyl trypt am mon ium chloride, C11H15N2 +·Cl-, (1), 2-methyl-1-phenyl trypt am mon ium chloride, C17H19N2 +·Cl-, (2), 5-meth oxy trypt am mon ium chloride, C11H15N2O+·Cl-, (3), 5-bromo trypt am mon ium chloride, C10H12BrN2 +·Cl-, (4), 5-chloro trypt am mon ium chloride, C10H12ClN2 +·Cl-, (5), 5-fluoro trypt am mon ium chloride, C10H12FN2 +·Cl-, (6), 5-methyl trypt am mon ium chloride, C11H15N2 +·Cl-, (7), 6-fluoro trypt am mon ium chloride, C10H12FN2 +·Cl-, (8), and 7-methyl trypt am mon ium chloride, C11H15N2 +·Cl-, (9), are reported. The seven tryptamines with N - H indoles, (3)-(9), show very similar structures, with N - H?Cl hydro gen-bonding networks forming two-dimensional sheets in the crystals. These sheets are combinations of R 4 2(8) and R 4 2(18) rings, and C 2 1(4) and C 2 1(9) chains. Substitution at the indole N atom reduces the dimensionality of the hydro gen-bonding network, with com pounds (1) and (2) demonstrating one-dimensional chains that are a combination of different rings and parallel chains.