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Ethanaminium, N,N,N-trimethyl-2-oxo-2-(phenylmethoxy)-, chloride is a complex organic compound with the chemical formula C11H16ClNO2. It is a derivative of ethanaminium, featuring a trimethylammonium group, a 2-oxo-2-(phenylmethoxy)-ethylidene moiety, and a chloride ion. Ethanaminium, N,N,N-trimethyl-2-oxo-2-(phenylmethoxy)-, chloride is characterized by its quaternary ammonium structure, which contributes to its potential applications in various chemical and pharmaceutical processes. The phenylmethoxy group provides a phenyl ring connected to an ether linkage, which may influence the compound's reactivity and solubility properties. Overall, this chemical is a member of the ethylammonium chlorides family and may be used in the synthesis of other organic compounds or as an intermediate in the production of pharmaceuticals.

3032-14-2

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3032-14-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3032-14-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,3 and 2 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3032-14:
(6*3)+(5*0)+(4*3)+(3*2)+(2*1)+(1*4)=42
42 % 10 = 2
So 3032-14-2 is a valid CAS Registry Number.

3032-14-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name trimethyl-(2-oxo-2-phenylmethoxyethyl)azanium,chloride

1.2 Other means of identification

Product number -
Other names benzyloxycarbonylmethyl-trimethyl-ammonium,chloride

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:3032-14-2 SDS

3032-14-2Downstream Products

3032-14-2Relevant academic research and scientific papers

Reactions with Betaines, XXIII. Reactions of Nitrogen- and Sulphur-Betaines with Reactive Halides

Wittmann, Helga,Ziegler, Erich

, p. 103 - 112 (2007/10/02)

Trimethylammonium acetic betain (1) reacts with phenacyl bromide and ethyl bromoacetate, respectively, to give the ester bromides 2 and 7.These can be hydrolyzed with aqueous sodium hydrogencarbonate at 20 deg C to yield besides 1 both C-benzoyl-methanol (3) and the glycolic acid ester 8, respectively.The reaction can also be performed in one step by reacting the betain (1) (with can act as a base) in a double molar ratio with the active halide. - Keywords: Trimethylammonium acetic acid betain; Trimethylammonium acetic acid phenacyl ester bromide; Trimethylammonium acetic acid acetoxy ethyl ester bromide; Phenacyl alcohol; Ethyl glycolate

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