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2040-37-1

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2040-37-1 Usage

Description

Benzene, [(1-phenylethoxy)methyl]is a chemical compound with the molecular formula C15H16O. It is a versatile building block in the synthesis of various pharmaceuticals and agrochemicals, and has potential antimicrobial and antioxidant properties. It is also being studied for its potential use in the development of new materials and compounds.

Uses

Used in Pharmaceutical Industry:
Benzene, [(1-phenylethoxy)methyl]is used as a building block for the synthesis of various pharmaceuticals. Its unique structure allows for the creation of new compounds with potential therapeutic applications.
Used in Agrochemical Industry:
Benzene, [(1-phenylethoxy)methyl]is used as a building block for the synthesis of agrochemicals. Its potential antimicrobial properties make it a valuable component in the development of new pesticides and other agricultural products.
Used in Material Science:
Benzene, [(1-phenylethoxy)methyl]is being studied for its potential use as a building block in the development of new materials and compounds. Its unique structure and properties may contribute to the creation of innovative materials with various applications.
However, it is important to note that exposure to Benzene, [(1-phenylethoxy)methyl]can pose health risks, including skin and eye irritation, and it is classified as a hazardous substance. Therefore, it should be handled with caution and in accordance with safety guidelines.

Check Digit Verification of cas no

The CAS Registry Mumber 2040-37-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,4 and 0 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2040-37:
(6*2)+(5*0)+(4*4)+(3*0)+(2*3)+(1*7)=41
41 % 10 = 1
So 2040-37-1 is a valid CAS Registry Number.

2040-37-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-phenylethoxymethylbenzene

1.2 Other means of identification

Product number -
Other names 1-phenylmethoxy-ethyl-benzene

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:2040-37-1 SDS

2040-37-1Relevant articles and documents

Organocatalysis Linked to Charge-Enhanced Acidity with Superelectrophilic Traits

Smajlagic, Ivor,White, Brandon,Azeez, Oyindamola,Pilkington, Melanie,Dudding, Travis

, p. 1128 - 1138 (2022/01/19)

Hydrogen bonding is ubiquitous throughout nature and serves as a versatile platform for accessing chemical reactivity. In leveraging this force, chemists have utilized organocatalysts to expand the spectrum of chemical reactivity enabled by hydrogen bondi

Intramolecular activation of imidate with cationic gold(I) catalyst: A new benzylation reaction of alcohols

Ban, Shintaro,Endo, Tomotake,Matsui, Rikako,Morita, Nobuyoshi,Hashimoto, Yoshimitsu,Tanaka, Kosaku,Tamura, Osamu

, (2020/08/28)

Benzylation of alcohols with benzyl (Z)-2,2,2-trifluoro-N-(2-alkynylphenyl)acetimidates 5a-f in the presence of a cationic gold(I) catalyst was investigated. Reagent 5f was the most effective, affording benzyl ethers in good yields. Our results indicate that these gold(I)-activated imidates are effective leaving groups.

Cp*CoIII-Catalyzed Efficient Dehydrogenation of Secondary Alcohols

Gangwar, Manoj Kumar,Dahiya, Pardeep,Emayavaramban, Balakumar,Sundararaju, Basker

supporting information, p. 2445 - 2448 (2018/09/10)

A novel, well-defined molecular Cp*CoIII complex was isolated and structurally characterized for the first time. The efficiency of this cobalt catalyst was demonstrated in the alcohol dehydrogenation and dehydrative coupling of secondary alcohols under mild conditions into ketones and ethers, respectively.

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