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Trimethyl-(3-oxo-3-phenyl-propyl)azanium, also known as 3-phenyl-N,N,N-trimethyl-3-oxopropylammonium, is an organic compound with the chemical formula C13H18NO. It is a derivative of a quaternary ammonium salt, featuring a trimethylammonium group attached to a 3-oxo-3-phenylpropyl chain. trimethyl-(3-oxo-3-phenyl-propyl)azanium is characterized by its amine-like properties and is often used in various chemical reactions and applications, such as in the synthesis of pharmaceuticals and other organic compounds. Its structure consists of a phenyl ring attached to a three-carbon chain, with one of the carbons being a carbonyl group (C=O) and the other end connected to the trimethylammonium group. This unique structure endows it with specific reactivity and properties that can be exploited in various chemical processes.

69267-23-8

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69267-23-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69267-23-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,2,6 and 7 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 69267-23:
(7*6)+(6*9)+(5*2)+(4*6)+(3*7)+(2*2)+(1*3)=158
158 % 10 = 8
So 69267-23-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H18NO/c1-13(2,3)10-9-12(14)11-7-5-4-6-8-11/h4-8H,9-10H2,1-3H3/q+1

69267-23-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name trimethyl-(3-oxo-3-phenylpropyl)azanium,bromide

1.2 Other means of identification

Product number -
Other names trimethyl-(3-oxo-3-phenyl-propyl)azanium

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:69267-23-8 SDS

69267-23-8Relevant academic research and scientific papers

Syntheses and evaluation of some Mannich bases derived from acetophenones against P388 lymphocytic leukemia and toxicological assessment of 3-dimethyl-amino-2-dimethylaminomethyl-1-(4-methoxyphenyl)-1-propanone dihydrochloride in rats

Dimmock,Shyam,Logan,Smith,Cross

, p. 471 - 477 (2007/10/02)

A number of analogues of 3-dimethylamino-2-dimethylaminomethyl-1-(4-methoxyphenyl)-1-propanone dihydrochloride (IIa) and related compounds which showed activity against P388 lymphocytic leukemia were prepared, and of the 16 analogues, three met the criterion for activity in this screen. The toxicity of IIa was examined in rats and either single dose of 25 mg/kg or nine daily doses of 12.5 mg/kg administered by the intraperitoneal route produced marked irritation and damage to the tissue with which it came into contact. Compound IIa did not show significant activity against eight other tumor systems.

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