1745-18-2 Usage
Description
3-(4-Chlorophenyl)-1-propene, also known as 4-chlorostyrene, is a chemical compound with the formula C9H9Cl. It is a colorless to pale yellow liquid with a sharp odor, insoluble in water but soluble in organic solvents. 3-(4-CHLOROPHENYL)-1-PROPENE is primarily used as an intermediate in the synthesis of various chemicals, including pharmaceuticals, agrochemicals, and dyes.
Uses
Used in Pharmaceutical Industry:
3-(4-Chlorophenyl)-1-propene is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, 3-(4-chlorophenyl)-1-propene serves as a precursor for the production of various agrochemicals, contributing to the development of effective pest control agents and other agricultural products.
Used in Dye Industry:
3-(4-Chlorophenyl)-1-propene is utilized as a starting material in the synthesis of dyes, enabling the creation of a wide range of colorants for various applications, including textiles, plastics, and printing inks.
Used in Polymer Resin Production:
3-(4-CHLOROPHENYL)-1-PROPENE is also used in the production of polymer resins, which are essential in the manufacturing of plastics and other polymer-based materials.
Used in Copolymer Synthesis:
3-(4-Chlorophenyl)-1-propene acts as a monomer in the synthesis of copolymers, which are used to create materials with specific properties tailored for various industrial applications.
As an Environmental Consideration:
Check Digit Verification of cas no
The CAS Registry Mumber 1745-18-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,4 and 5 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1745-18:
(6*1)+(5*7)+(4*4)+(3*5)+(2*1)+(1*8)=82
82 % 10 = 2
So 1745-18-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H9Cl/c1-2-3-8-4-6-9(10)7-5-8/h2,4-7H,1,3H2
1745-18-2Relevant articles and documents
REACTION OF ARYL- AND VINYLSTANNANES WITH ALLYL ACETATE IN THE PRESENCE OF TETRAKIS(TRIPHENYLPHOSPHINE)PALLADIUM(0)
Beletskaya, I. P.,Kasatkin, A. N.,Lebedev, S. A.,Bumagin, N. A.
, p. 1994 (1981)
-
Manganese catalyzed dehydrogenative silylation of alkenes: Direct access to allylsilanes
Wu, Shang,Zhang, Ying,Jiang, Hongyan,Ding, Ning,Wang, Yanbin,Su, Qiong,Zhang, Hong,Wu, Lan,Yang, Quanlu
supporting information, (2020/06/03)
Dehydrogenative silylation of alkenes with silanes to produce allylsilanes is achieved through manganese catalysis with a wide scope of substrate tolerance. This transformation involves silane radicals initiated by manganese complex without additional oxidant additives. It offers a general, convenient and practical protocol with excellent functional group compatibility and gram-scale capacity for the modular synthesis of allylsilanes.
Palladium-Catalyzed Oxidative Allylation of Sulfoxonium Ylides: Regioselective Synthesis of Conjugated Dienones
Li, Chunsheng,Li, Meng,Zhong, Wentao,Jin, Yangbin,Li, Jianxiao,Wu, Wanqing,Jiang, Huanfeng
supporting information, p. 872 - 875 (2019/05/16)
The first examples of palladium-catalyzed allylic C-H oxidative allylation of sulfoxonium ylides to afford the corresponding conjugated dienones with moderate to good yields have been established. The features of this novel conversion include mild reaction conditions, wide substrate scope, and excellent regioselectivity.
