7318-34-5 Usage
Uses
Used in Pharmaceutical Industry:
1-(4-chlorobut-2-en-1-yl)-2-nitrobenzene is used as a starting material for the synthesis of various pharmaceutical compounds. Its unique structure allows for the creation of a wide array of medicinally relevant molecules, contributing to the development of new drugs and therapies.
Used in Agrochemical Industry:
In the agrochemical industry, 1-(4-chlorobut-2-en-1-yl)-2-nitrobenzene serves as a key starting material for the synthesis of different agrochemicals. Its versatility in organic synthesis enables the production of compounds that can be utilized in the development of pesticides, herbicides, and other agricultural products.
Used in Research and Laboratory Settings:
1-(4-chlorobut-2-en-1-yl)-2-nitrobenzene is employed as a research compound in various scientific investigations. Its ability to undergo a range of chemical reactions makes it a valuable tool for exploring new reaction pathways and synthesizing novel derivatives. 1-(4-chlorobut-2-en-1-yl)-2-nitrobenzene's potential applications in research can lead to advancements in both pharmaceutical and agrochemical fields.
Check Digit Verification of cas no
The CAS Registry Mumber 7318-34-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,1 and 8 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7318-34:
(6*7)+(5*3)+(4*1)+(3*8)+(2*3)+(1*4)=95
95 % 10 = 5
So 7318-34-5 is a valid CAS Registry Number.
7318-34-5Relevant academic research and scientific papers
2-(2-aminophenyl)-acetaldehyde dimethyl acetal: A novel reagent for the protection of carboxylic acids
Arai, Eri,Tokuyama, Hidetoshi,Linsell, Martin S.,Fukuyama, Tohru
, p. 71 - 74 (2007/10/03)
The synthesis and use of 2-(2-aminophenyl)-acetaldehyde dimethyl acetal 1 are described. The amides 2, derived from this amine and carboxylic acids, are stable under basic conditions and thus can be regarded as the protected carboxylic acids. The corresponding carboxylic acids are regenerated by conversion of 2 into indolylamides 3 by treatment with CSA and subsequent hydrolysis with LiOOH or NaOH. In addition, 3 can be easily converted to esters, amides, and aldehydes.
