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Benzenemethanaminium, N-(2-ethoxy-2-oxoethyl)-N,N-dimethyl-, bromide is a complex organic compound with the chemical formula C12H20BrNO2. It is a derivative of benzenemethanaminium, featuring a dimethylamino group and a 2-ethoxy-2-oxoethyl group attached to the benzene ring. The compound is characterized by its bromide salt form, which contributes to its ionic nature. This chemical is primarily used in the synthesis of various pharmaceuticals and organic compounds due to its unique structure and reactivity. It is important to handle this substance with care, as it may have potential health and environmental impacts, and is typically used in a controlled laboratory setting by professionals.

61532-94-3

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61532-94-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61532-94-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,5,3 and 2 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 61532-94:
(7*6)+(6*1)+(5*5)+(4*3)+(3*2)+(2*9)+(1*4)=113
113 % 10 = 3
So 61532-94-3 is a valid CAS Registry Number.

61532-94-3SDS

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 Benzyldimethylammonium-essigsaeureethylester-bromid

1.2 Other means of identification

Product number -
Other names ethoxycarbonylmethyl-benzyl-dimethyl-ammonium, bromide

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:61532-94-3 SDS

61532-94-3Relevant academic research and scientific papers

The Influence of Substituents at the Cationic Center of Betaines on the Tendency of Formation of Di-trifluoracetyl N-Ylides

Ziegler, Erich,Wittmann, Helga

, p. 821 - 830 (2007/10/02)

The influence of substituents at the ammonium nitrogen of acetic acid betaines on the reaction with trifluoroacetic anhydride (TFA) has been investigated.Thus benzyl-dimethyl- and phenyl-dimethyl-betaines (1a, 1b) as well as the bifunctional betaines deri

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