304-47-2

Basic information

• Product Name: KYNURAMINE DIHYDROBROMIDE
• Synonyms: KYNURAMINE DIHYDROBROMIDE;3-[2-AMINOPHENYL]-3-OXOPROPANAMINE DIHYDROBROMIDE;3-(2-aminophenyl)-3-oxopropanamine;3-aMino-1-(2-aMinophenyl)propan-1-one dihydrobroMide
• CAS NO: 304-47-2
• Molecular Formula: C9H14Br2N2O
• Molecular Weight: 326.03
• Mol File: 304-47-2.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 367.3°Cat760mmHg
• Flash Point: 175.9°C
• Appearance: light yellow/crystalline
• Density: g/cm³
• Vapor Pressure: 7.57E-06mmHg at 25°C
• Storage Temp.: −20°C
• CAS DataBase Reference: KYNURAMINE DIHYDROBROMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: KYNURAMINE DIHYDROBROMIDE(304-47-2)
• EPA Substance Registry System: KYNURAMINE DIHYDROBROMIDE(304-47-2)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 304-47-2(Hazardous Substances Data)

Usage

Uses

Kynuramine dihydrobromide has been used as a substrate for monoamine oxidase.

Biochem/physiol Actions

Kynuramine dihydrobromide is a substrate for the enzyme monoamine oxidase. The end product is the formation of fluorescence detectable 4-hydroxyquinoline (4-HOQ) measured in a fluorescence spectrophotometer at 380 nm.

InChI:InChI=1/C9H12N2O.BrH/c10-6-5-9(12)7-3-1-2-4-8(7)11;/h1-4H,5-6,10-11H2;1H

Upstream product

• 63637-61-6 kynuramine methyl carbamate 
• 61-54-1 tryptamine 
• 58635-45-3 methyl 2-(1-H-indol-3-yl)ethylcarbamate 
• 77516-15-5 2,3-dihydro-Nb-methoxycarbonyl-2-oxotriptamine 
• 343-94-2 tryptamine hydochloride 

Downstream Products

• 113321-71-4 cystodytin A 
• 1430088-65-5 styelsamine-N¹⁴-benzamide 
• 1430088-69-9 cystodytin-N¹⁴-benzamide 
• 1430088-66-6 styelsamine-N¹⁴-2-phenylacetamide 
• 1430088-70-2 cystodytin-N¹⁴-2-phenylacetamide 
• 1430088-67-7 styelsamine-N¹⁴-3-phenylpropanamide 
• 1430088-71-3 cystodytin-N¹⁴-3-phenylpropanamide 
• 1430088-76-8 O-methyl styelsamine-N¹⁴-2-phenylacetamide 
• 1430088-78-0 O-methyl styelsamine-N¹⁴-3-phenylpropanamide 
• 86047-14-5 amphimedine 

Relevant articles and documents

Bioinspired Syntheses of the Pyridoacridine Marine Alkaloids Demethyldeoxyamphimedine, Deoxyamphimedine, and Amphimedine

Efficient bioinspired syntheses of the biologically active pyridoacridine marine alkaloids demethyldeoxyamphimedine, deoxyamphimedine, and amphimedine are reported. Reaction of styelsamine D, prepared via an optimized route starting from Boc-dopamine, wit

A simple biomimetic synthesis of styelsamine B.

An extremely rapid, low cost, and environmentally friendly entry into the pyridoacridine family of alkaloids has been devised, as demonstrated here by the first total synthesis of styelsamine B (3) and its oxidation to the quinoneimine cystodytin J (4). T