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2-[6-(3,5-dimethoxyphenyl)-3-oxohexyl]-2-ethylcyclopentane-1,3-dione is a complex organic compound with a molecular formula of C21H28O6. It is characterized by a cyclopentane-1,3-dione core, which is a five-membered ring with two carbonyl groups (C=O) at positions 1 and 3. Attached to this core is a 6-(3,5-dimethoxyphenyl)-3-oxohexyl chain, which includes a 3-oxohexyl group (a hexyl chain with a carbonyl group at the third position) and a 3,5-dimethoxyphenyl group (a phenyl ring with two methoxy groups at the 3rd and 5th positions). Additionally, the compound has an ethyl group attached to the 2-position of the cyclopentane ring. This chemical structure suggests potential applications in pharmaceuticals or as a synthetic intermediate, given its intricate arrangement of functional groups.

4244-18-2

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4244-18-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4244-18-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,4 and 4 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4244-18:
(6*4)+(5*2)+(4*4)+(3*4)+(2*1)+(1*8)=72
72 % 10 = 2
So 4244-18-2 is a valid CAS Registry Number.

4244-18-2Downstream Products

4244-18-2Relevant 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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