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2-(6-m-methoxyphenyl-3-oxohexyl)-2-methylcyclohexane-1,3-dione is a complex organic compound with a molecular formula of C19H24O4. It is characterized by a cyclohexane ring with a 1,3-dione functional group, a methyl group, and a 6-m-methoxyphenyl-3-oxohexyl side chain. The compound's structure features a phenyl ring with a methoxy group at the meta position, attached to a hexyl chain that includes a ketone group. This molecule is likely to be found in the field of organic chemistry, potentially as an intermediate in the synthesis of pharmaceuticals or other complex organic molecules. Its specific applications and properties would depend on its reactivity, stability, and the context in which it is used.

1424-75-5

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1424-75-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1424-75-5 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 5 respectively.
Calculate Digit Verification of CAS Registry Number 1424-75:
(6*1)+(5*4)+(4*2)+(3*4)+(2*7)+(1*5)=65
65 % 10 = 5
So 1424-75-5 is a valid CAS Registry Number.

1424-75-5Relevant 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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