15422-18-1 Usage
Description
1-(3-CHLOROPHENOXY)-2-PROPANONE, with the molecular formula C9H9ClO2, is a pale yellow liquid chemical compound characterized by a molecular weight of 184.62 g/mol. It is known for its utility as an intermediate in the synthesis of pharmaceuticals and agrochemicals, as well as a chemical building block in organic synthesis. Additionally, it is employed in the production of perfumes and flavorings, with its chlorophenyl group contributing to the development of various organic compounds. However, it is crucial to handle this compound with proper safety measures due to its potential hazards if mismanaged.
Uses
Used in Pharmaceutical Industry:
1-(3-CHLOROPHENOXY)-2-PROPANONE is used as an intermediate for the synthesis of various pharmaceutical compounds, contributing to the development of new drugs and medications.
Used in Agrochemical Industry:
In the agrochemical sector, 1-(3-CHLOROPHENOXY)-2-PROPANONE serves as an intermediate in the production of agrochemicals, which are essential for enhancing crop protection and agricultural productivity.
Used in Organic Synthesis:
1-(3-CHLOROPHENOXY)-2-PROPANONE is utilized as a chemical building block in organic synthesis, playing a vital role in the creation of diverse organic compounds.
Used in Perfume and Flavoring Industry:
1-(3-CHLOROPHENOXY)-2-PROPANONE is also employed in the production of perfumes and flavorings, where its unique properties contribute to the development of distinct scents and tastes.
Check Digit Verification of cas no
The CAS Registry Mumber 15422-18-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,4,2 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 15422-18:
(7*1)+(6*5)+(5*4)+(4*2)+(3*2)+(2*1)+(1*8)=81
81 % 10 = 1
So 15422-18-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H9ClO2/c1-7(11)6-12-9-4-2-3-8(10)5-9/h2-5H,6H2,1H3
15422-18-1Relevant articles and documents
Selective Cross-Dehydrogenative C(sp3)-H Arylation with Arenes
Hao, Hong-Yan,Mao, Yang-Jie,Xu, Zhen-Yuan,Lou, Shao-Jie,Xu, Dan-Qian
supporting information, p. 2396 - 2402 (2020/03/13)
Selective C(sp3)-C(sp2) bond construction is of central interest in chemical synthesis. Despite the success of classic cross-coupling reactions, the cross-dehydrogenative coupling between inert C(sp3)-H and C(sp2)-H bonds represents an attractive alternative toward new C(sp3)-C(sp2) bonds. Herein, we establish a selective inter-and intramolecular C(sp3)-H arylation of alcohols with nondirected arenes that thereby provides a general pathway to access a wide range of β-arylated alcohols, including tetrahydronaphthalen-2-ols and benzopyran-3-ols, with high to excellent chemo-and regioselectivity.
A (different) bright ammonia amide carbamate derivative and application thereof (by machine translation)
-
Paragraph 0036; 0037; 0038; 0045; 0046, (2017/07/14)
The invention belongs to the field of plant, relates to a general formula (I) is shown in a (different) bright ammonia amide carbamate derivatives and their pharmaceutically acceptable salt, wherein substituent R has the definition given in the specification, the invention also relates to the general formula (I) preparation of compounds of the, specifically for the preparation of the intermediate of its development and application of plant disease control. (by machine translation)
