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"δ-Hydroxy-δ-phenyl-δ-p-fluorophenylbutyl chloride" is a complex organic chemical compound with the molecular formula C15H15ClFO. It is characterized by the presence of a hydroxyl group (-OH), a phenyl ring (C6H5), and a p-fluorophenyl group (C6H4F) attached to a butyl chain (C4H9). The compound's structure features a chlorine atom (Cl) at the δ (delta) position, which is the third carbon atom from the end of the butyl chain. This specific arrangement of functional groups and atoms gives the compound unique chemical properties and potential applications in various fields, such as pharmaceuticals or chemical research.

77294-14-5

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77294-14-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77294-14-5 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 4 respectively.
Calculate Digit Verification of CAS Registry Number 77294-14:
(7*7)+(6*7)+(5*2)+(4*9)+(3*4)+(2*1)+(1*4)=155
155 % 10 = 5
So 77294-14-5 is a valid CAS Registry Number.

77294-14-5Relevant 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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