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2-(6-m-acetoxyphenyl-3-oxohexyl)-2-methylcyclopentane-1,3-dione is a complex organic compound with a molecular formula of C19H24O5. It is characterized by a cyclopentane ring, which is a five-membered ring structure, and a 3-oxohexyl chain that is connected to a 6-m-acetoxyphenyl group. The compound features a methyl group attached to the cyclopentane ring and a 1,3-dione functional group, indicating the presence of two carbonyl groups (C=O) separated by a single carbon atom. The 6-m-acetoxyphenyl group introduces an acetoxy substituent on the meta position of the phenyl ring, which can influence the compound's reactivity and physical properties. This chemical structure is likely to be found in specialized applications, such as in the synthesis of pharmaceuticals or as an intermediate in organic chemistry, due to its unique arrangement of functional groups and potential for further reactions.

4244-16-0

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4244-16-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4244-16-0 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 6 respectively.
Calculate Digit Verification of CAS Registry Number 4244-16:
(6*4)+(5*2)+(4*4)+(3*4)+(2*1)+(1*6)=70
70 % 10 = 0
So 4244-16-0 is a valid CAS Registry Number.

4244-16-0Downstream Products

4244-16-0Relevant 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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