937-61-1 Usage
Description
(propoxymethyl)benzene, also known as p-isopropoxymethylbenzene, is a chemical compound with the formula C10H14O. It is a colorless to pale yellow liquid with a faint, sweet odor and is recognized for its versatile applications across various industries.
Uses
Used in the Paint and Coatings Industry:
(propoxymethyl)benzene is used as a solvent for its ability to dissolve and carry other substances, which is crucial in the production of paints, coatings, and similar products. Its solvent properties enhance the manufacturing process and contribute to the final product's quality.
Used in the Adhesives Industry:
In the adhesives industry, (propoxymethyl)benzene serves as a solvent that helps in the formulation of adhesives, improving their bonding capabilities and overall performance.
Used in the Flavor and Fragrance Industry:
(propoxymethyl)benzene is utilized as a flavor and fragrance ingredient, adding to the sensory experience of household and personal care products. Its sweet odor makes it a valuable component in creating pleasant scents for consumer products.
Used in the Pharmaceutical Industry:
As an intermediate in the synthesis of pharmaceuticals, (propoxymethyl)benzene plays a significant role in the development of various medications, contributing to the advancement of healthcare and medical treatments.
Used in the Agricultural Chemicals Industry:
Similarly, (propoxymethyl)benzene is employed as an intermediate in the synthesis of agricultural chemicals, aiding in the production of substances that are essential for the farming industry, such as pesticides and fertilizers.
Caution:
It is important to handle (propoxymethyl)benzene with care, as it may cause skin and eye irritation. Additionally, it is harmful if ingested or inhaled, necessitating proper safety measures during its use and storage.
Check Digit Verification of cas no
The CAS Registry Mumber 937-61-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,3 and 7 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 937-61:
(5*9)+(4*3)+(3*7)+(2*6)+(1*1)=91
91 % 10 = 1
So 937-61-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H14O/c1-2-8-11-9-10-6-4-3-5-7-10/h3-7H,2,8-9H2,1H3
937-61-1Relevant articles and documents
Selective alkene hydrogenation with atomic hydrogen permeating through a Pd sheet electrode
Maki,Harada,Hirano,Niwa,Yoshida,Ogata,Nakamatsu,Inoue,Iwakura
, p. 3575 - 3583 (2000)
Chemoselective hydrogenation of olefinic double bonds without concomitant hydrogenolysis of allylic and benzylic C-O linkages was performed successfully by the aid of active hydrogen permeated through a Pd sheet electrode.
Method for hydrogenolysis of halides
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Paragraph 0232; 0281-0283, (2021/01/11)
The invention discloses a method for hydrogenolysis of halides. The invention discloses a preparation method of a compound represented by a formula I. The preparation method comprises the following step: in a polar aprotic solvent, zinc, H2O and a compound represented by a formula II are subjected to a reaction as shown in the specification, wherein X is halogen; Y is -CHRR or R; hydrogenin H2O exists in the form of natural abundance or non-natural abundance. According to the preparation method, halide hydrogenolysis can be simply, conveniently and efficiently achieved through a simple and mild reaction system, and good functional group compatibility and substrate universality are achieved.
Dehalogenative Deuteration of Unactivated Alkyl Halides Using D2O as the Deuterium Source
Xia, Aiyou,Xie, Xin,Hu, Xiaoping,Xu, Wei,Liu, Yuanhong
, p. 13841 - 13857 (2019/10/17)
The general dehalogenation of alkyl halides with zinc using D2O or H2O as a deuterium or hydrogen donor has been developed. The method provides an efficient and economic protocol for deuterium-labeled derivatives with a wide substrate scope under mild reaction conditions. Mechanistic studies indicated that a radical process is involved for the formation of organozinc intermediates. The facile hydrolysis of the organozinc intermediates provides the driving force for this transformation.
