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304-47-2

KYNURAMINE DIHYDROBROMIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 304-47-2 Structure

  • Basic information

    1. Product Name: KYNURAMINE DIHYDROBROMIDE
    2. Synonyms: KYNURAMINE DIHYDROBROMIDE;3-[2-AMINOPHENYL]-3-OXOPROPANAMINE DIHYDROBROMIDE;3-(2-aminophenyl)-3-oxopropanamine;3-aMino-1-(2-aMinophenyl)propan-1-one dihydrobroMide
    3. CAS NO:304-47-2
    4. Molecular Formula: C9H14Br2N2O
    5. Molecular Weight: 326.03
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 304-47-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 367.3°Cat760mmHg
    3. Flash Point: 175.9°C
    4. Appearance: light yellow/crystalline
    5. Density: g/cm3
    6. Vapor Pressure: 7.57E-06mmHg at 25°C
    7. Refractive Index: N/A
    8. Storage Temp.: −20°C
    9. Solubility: N/A
    10. CAS DataBase Reference: KYNURAMINE DIHYDROBROMIDE(CAS DataBase Reference)
    11. NIST Chemistry Reference: KYNURAMINE DIHYDROBROMIDE(304-47-2)
    12. EPA Substance Registry System: KYNURAMINE DIHYDROBROMIDE(304-47-2)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 304-47-2(Hazardous Substances Data)

304-47-2 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.

Check Digit Verification of cas no

The CAS Registry Mumber 304-47-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,0 and 4 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 304-47:
(5*3)+(4*0)+(3*4)+(2*4)+(1*7)=42
42 % 10 = 2
So 304-47-2 is a valid CAS Registry Number.
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

304-47-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name Kynuramine dihydrobromide

1.2 Other means of identification

Product number -
Other names 3-(2-Aminophenyl)-3-oxopropanamine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:304-47-2 SDS

304-47-2Relevant articles and documents

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

Khalil, Iman M.,Barker, David,Copp, Brent R.

, p. 282 - 289 (2016/01/15)

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

Synthesis, DNA binding and antitumor evaluation of styelsamine and cystodytin analogues

Fong, Hugo K.H.,Copp, Brent R.

, p. 274 - 299 (2013/05/21)

A series of N-14 sidechain substituted analogues of styelsamine (pyrido[4,3,2-mn]acridine) and cystodytin (pyrido[4,3,2-mn]acridin-4-one) alkaloids have been prepared and evaluated for their DNA binding affinity and antiproliferative activity towards a pa

A simple biomimetic synthesis of styelsamine B.

Skyler,Heathcock

, p. 4323 - 4324 (2007/10/03)

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

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