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"δ-Hydroxy-δ-methyl-δ-p-fluorophenylbutyl chloride" is a complex organic chemical compound with the molecular formula C11H14ClFO. It is characterized by the presence of a hydroxyl group (-OH), a methyl group (-CH3), and a p-fluorophenyl group (C6H4F) attached to a butyl chain (C4H9). The compound's structure features a chlorine atom (Cl) attached to the terminal carbon atom of the butyl chain, making it a chlorinated derivative. This chemical is primarily used in the synthesis of various pharmaceuticals and agrochemicals due to its unique structural properties and reactivity.

77294-13-4

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77294-13-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77294-13-4 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 3 respectively.
Calculate Digit Verification of CAS Registry Number 77294-13:
(7*7)+(6*7)+(5*2)+(4*9)+(3*4)+(2*1)+(1*3)=154
154 % 10 = 4
So 77294-13-4 is a valid CAS Registry Number.

77294-13-4Relevant 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.

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