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The chemical compound "13-methyl-3-propoxy-7,8,9,11,12,13,15,16-octahydro-6H-cyclopenta[a]phenanthren-17(14H)-one" is a complex organic molecule with a molecular formula of C21H28O2. It belongs to the class of compounds known as cyclopenta[a]phenanthrenes, which are a type of polycyclic aromatic hydrocarbons. This specific compound features a cyclopenta[a]phenanthrene core with a methyl group at the 13th position, a propoxy group at the 3rd position, and an additional hydroxyl group at the 17th position. The compound is characterized by its octahydro structure, indicating the presence of eight hydrogen atoms in a saturated ring system. It is a white crystalline solid and is used in various chemical and pharmaceutical applications due to its unique structure and properties.

1852-86-4

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1852-86-4 Usage

Molecular structure

Contains a cyclopentane ring and a phenanthrene ring.

Classification

Steroid derivative.

Pharmacological activities

Anti-inflammatory and immunomodulatory effects.

Origin

Likely a synthetic derivative of natural steroid hormones.

Potential applications

Medicinal and pharmaceutical uses.

Research status

Further research needed to fully understand and harness its potential.

Check Digit Verification of cas no

The CAS Registry Mumber 1852-86-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,5 and 2 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1852-86:
(6*1)+(5*8)+(4*5)+(3*2)+(2*8)+(1*6)=94
94 % 10 = 4
So 1852-86-4 is a valid CAS Registry Number.

1852-86-4Downstream Products

1852-86-4Relevant academic research and scientific papers

Enhanced Reactivity of Aerobic Diimide Olefin Hydrogenation with Arylboronic Compounds: An Efficient One-Pot Reduction/Oxidation Protocol

Santra, Surojit,Guin, Joyram

supporting information, p. 7253 - 7257 (2015/11/25)

A catalyst-free and efficient method for simultaneous olefin hydrogenation and oxidation of arylboronate esters to phenols with hydrazine hydrate and molecular oxygen is presented. The process is based on the utilization of a readily available Lewis acidic arylboron compound, which evades common problems associated with the catalyst-free aerobic hydrogenation of olefins with diimide. Using an operationally simple procedure, the protocol smoothly delivers phenol derivatives and various alkanes in excellent yields with remarkable functional group compatibility. The method allows the reaction to be scaled up to 1 g of the starting materials.

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