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1-Diethylamino-6-m-acetoxyphenylhex-2-yne is a complex organic compound with the molecular formula C18H23NO2. It features a hex-2-yne backbone, which is a six-carbon chain with a triple bond between the second and third carbon atoms. The molecule also contains a diethylamino group (N-(C2H5)2) attached to the first carbon, and a para-acetoxyphenyl group (O-CO-CH3 attached to a phenyl ring) at the sixth carbon. The para-acetoxyphenyl group is characterized by the acetoxy (O-CO-CH3) substituent being located on the para position (four carbons away) relative to the point of attachment on the phenyl ring. 1-diethylamino-6-m-acetoxyphenylhex-2-yne is known for its unique structure and potential applications in various chemical and pharmaceutical industries.

1971-85-3

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1971-85-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1971-85-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,7 and 1 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1971-85:
(6*1)+(5*9)+(4*7)+(3*1)+(2*8)+(1*5)=103
103 % 10 = 3
So 1971-85-3 is a valid CAS Registry Number.

1971-85-3Downstream Products

1971-85-3Relevant 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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