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Benzenemethanaminium, 4-benzoyl-N-dodecyl-N,N-dimethyl-, bromide is a complex organic compound with the chemical formula C21H34BrNO. It is a derivative of benzenemethanaminium, featuring a benzoyl group at the 4-position, a dodecyl chain, and two methyl groups attached to the nitrogen atom. Benzenemethanaminium, 4-benzoyl-N-dodecyl-N,N-dimethyl-, bromide is characterized by its cationic nature, which makes it a potential candidate for applications in various fields, such as pharmaceuticals, agrochemicals, and materials science. The bromide salt form suggests that it can be used as a precursor for the synthesis of other compounds or as a reagent in chemical reactions. Its specific properties and applications would depend on the context in which it is used, and further research would be needed to explore its potential uses and effects.

74386-45-1

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74386-45-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74386-45-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,3,8 and 6 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 74386-45:
(7*7)+(6*4)+(5*3)+(4*8)+(3*6)+(2*4)+(1*5)=151
151 % 10 = 1
So 74386-45-1 is a valid CAS Registry Number.

74386-45-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-benzoylphenyl)methyl-dodecyl-dimethylazanium,bromide

1.2 Other means of identification

Product number -
Other names Benzenemethanaminium,4-benzoyl-N-dodecyl-N,N-dimethyl-,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:74386-45-1 SDS

74386-45-1Downstream Products

74386-45-1Relevant academic research and scientific papers

ANTIBACTERIAL HYDROPHILIC COMPOUND AND USE THEREOF

-

, (2020/04/10)

The present disclosure provides an antibacterial hydrophilic compound. The antibacterial hydrophilic compound may react, induced by light through a hydrogen abstraction group in the structural formula thereof, with a C—H group and thus bind to a surface of a material having the C—H group (for example, chemical fibers such as polyester, chinlon, and the like; plastics, rubbers, and other similar materials), which can impart a durable antibacterial activity and hydrophilicity to the material. The antibacterial hydrophilic compound has a relatively strong binding force to the surface of the material without damaging the mechanical properties of the raw material. The present disclosure also provides a modified material that is modified by the antibacterial hydrophilic compound.

UNEXPECTED HIGH PHOTOIXIDIZING EFFICIENCY OF BENZOPHENONE DERIVATIVES HAVING TETRAALKYLAMMONIUM SUBSTITUENTS

Tazuke, Shigeo,Kawasaki, Yasuhiro,Kitamura, Noboru,Inoue, Takashi

, p. 251 - 254 (2007/10/02)

Benzophenone derivatives having various tetraalkylammonium ion in the 4 position (II, III, IV, and V) were found to be much more efficient senzitizers than benzophenone(I) in photooxidation of Leuco Crystal Violet(LCV) to Crystal Violet(CV+) in acetonitrile in air, which was interpreted in terms of the cationic atmosphere effect facilitating the primary electron transfer process from LCV to BP*3.

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