77294-15-6 Usage
Uses
Used in Pharmaceutical Industry:
1-(4-chloro-1-methyl-1-butenyl)-4-fluorobenzene is used as a key intermediate for the synthesis of pharmaceuticals. Its unique chemical structure allows it to be a valuable building block in the creation of new and existing medications, contributing to the development of novel therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, 1-(4-chloro-1-methyl-1-butenyl)-4-fluorobenzene is utilized as a starting material for the production of various agrochemicals. Its role in this industry is essential for the development of new compounds that can help improve crop protection and yield.
Used in Chemical Production:
1-(4-chloro-1-methyl-1-butenyl)-4-fluorobenzene is also employed as an intermediate in the production of a wide range of chemicals, including dyes, polymers, and fragrances. Its versatility and reactivity make it a crucial component in the synthesis of these diverse products.
Safety Note:
Due to its flammable nature, 1-(4-chloro-1-methyl-1-butenyl)-4-fluorobenzene should be handled with care to avoid potential hazards. Proper safety measures and precautions must be taken during its use in various applications to ensure the safety of personnel and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 77294-15-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,2,9 and 4 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 77294-15:
(7*7)+(6*7)+(5*2)+(4*9)+(3*4)+(2*1)+(1*5)=156
156 % 10 = 6
So 77294-15-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H12ClF/c1-9(3-2-8-12)10-4-6-11(13)7-5-10/h3-7H,2,8H2,1H3/b9-3+
77294-15-6Relevant academic research and scientific papers
Agents Acting on CNS: Part XXX - Synthesis of 2-Substituted 1,2,3,4,6,7,12,12a-Octahydropyrazinopyrido-indoles
Dhaon, Madhup K.,Kumar, Naresh,Agarwal, Shiv K.,Saxena, Anil K.,Jain, Padam C.,Anand, Nitya
, p. 882 - 885 (2007/10/02)
A number of 2-substituted pyrazinopyridoindoles (3,6-12) have been prepared by the condensation of 1,2,3,4,6,7,12,12a-octahydropyrazinopyridoindole (1) with appropriate halogen compounds.Treatment of 1 with ethylene oxide gives 4 which on condensation with p-fluorobenzoyl chloride yields 5.The corresponding 2-γ-(p-fluorobenzoyl)propyl-6-oxo-octahydropyrazinopyridoindole (14) is prepared by the oxidation of 1 with mercuric acetate followed by condensation of the resulting 6-oxo derivative (13) with γ-chloro-p-fluorobutyrophenone. 1-Oxo-2-substituted-pyrazinopyridoindoles (16-18) are prepared by the reaction of ethylene oxide on methyl 1,2,3,4-tetrahydropyridoindole-3-carboxylate followed by condensation of the resulting oxazino derivative (15) with amines.These compounds show tranquillizing, anti-inflammatory and diuretic activities.