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2-[6-(3,4-Dimethoxy-phenyl)-3-oxo-hexyl]-2-ethyl-cyclopentane-1,3-dione is a complex organic compound with a molecular formula of C21H26O6. 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 2-ethyl group and a 6-(3,4-dimethoxy-phenyl)-3-oxo-hexyl chain. The latter chain features a 3,4-dimethoxy-phenyl group, which includes two methoxy (OCH3) substituents on the phenyl ring, and a 3-oxo-hexyl group, indicating a six-carbon chain with a carbonyl group at the third position. 2-[6-(3,4-Dimethoxy-phenyl)-3-oxo-hexyl]-2-ethyl-cyclopentane-1,3-dione is likely to be found in the realm of pharmaceuticals or as an intermediate in the synthesis of various organic compounds due to its intricate structure and functional groups.

4244-03-5

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4244-03-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4244-03-5 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, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4244-03:
(6*4)+(5*2)+(4*4)+(3*4)+(2*0)+(1*3)=65
65 % 10 = 5
So 4244-03-5 is a valid CAS Registry Number.

4244-03-5Downstream Products

4244-03-5Relevant academic research and scientific papers

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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