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1-Diethylamino-6-phenylhex-2-yne is an organic compound characterized by its unique molecular structure, which consists of a hex-2-yne backbone with a diethylamino group at the 1st position and a phenyl group at the 6th position. 1-diethylamino-6-phenylhex-2-yne is a derivative of alkynes, which are hydrocarbons with a carbon-carbon triple bond. The presence of the diethylamino group introduces a nitrogen atom bonded to two ethyl groups, while the phenyl group adds an aromatic ring to the molecule. This combination of functional groups gives 1-diethylamino-6-phenylhex-2-yne distinct chemical properties, making it a potentially useful building block in the synthesis of more complex organic molecules.

1424-72-2

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1424-72-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1424-72-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,2 and 4 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1424-72:
(6*1)+(5*4)+(4*2)+(3*4)+(2*7)+(1*2)=62
62 % 10 = 2
So 1424-72-2 is a valid CAS Registry Number.

1424-72-2Relevant academic research and scientific papers

Synthesis of gon-4-enes

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, (2008/06/13)

1. A therapeutic composition having progestational activity comprising as active ingredient a 17-aliphatic carboxylic acid ester of 17α-ethynyl-18-methyl-19-nortestosterone and a pharmaceutical carrier for said compound.

Synthesis of 13-alkyl-gon-4-ones

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, (2008/06/13)

The preparation of 13-methylgon-4-enes and novel 13-polycarbonalkylgon-4-enes by a new total synthesis is described. 13-Alkylgon-4-enes having progestational, anabolic and androgenic activities are prepared by forming a tetracylic gonane structure unsaturated in the 1,3,5(10),9(11) and 14-positions, selectively reducing in the B- and C-rings, and converting the aromatic A-ring compounds so-produced to gon-4-enes by Birch reduction and hydrolysis.

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