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14-methylcholest-7-en-3-yl acetate is a chemical compound derived from cholesterol, specifically a cholestane derivative. It is characterized by the presence of a methyl group at the 14th carbon position and a double bond between the 7th and 8th carbon atoms in the steroid nucleus. The compound is further modified by the acetylation of the 3-hydroxyl group, resulting in the formation of an ester linkage. This modification can influence the compound's solubility, reactivity, and biological activity. 14-methylcholest-7-en-3-yl acetate is primarily used in research and pharmaceutical applications, where it may serve as an intermediate in the synthesis of other steroidal compounds or as a probe for studying biological processes involving cholesterol and its derivatives.

5259-20-1

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5259-20-1 Usage

Chemical class

Steroids and steroid derivatives

Source

Derived from cholesterol and commonly found in plants

Industrial applications

Pharmaceuticals, cosmetics, and perfumery

Biological properties

Exhibits anti-inflammatory and anti-cancer activities

Therapeutic potential

Valuable ingredient in the development of new drugs for the treatment of various diseases

Fragrance use

Utilized as a fragrance ingredient in perfumes and skincare products due to its pleasant odor

Molecular weight

Approximately 456.7 g/mol (calculated from the molecular formula)

Appearance

Likely a solid or viscous liquid, depending on the conditions (inferred from the structure and molecular weight)

Solubility

Likely soluble in organic solvents such as ethanol, methanol, or acetone (inferred from the structure and typical solubility of steroid derivatives)

Stability

Stable under normal conditions, but sensitive to heat, light, and oxidation (inferred from the structure and typical stability of steroid derivatives)

Reactivity

May react with strong acids, strong bases, or oxidizing agents (inferred from the structure and typical reactivity of steroid derivatives)

Toxicity

Information on toxicity is not provided in the material, but it is important to consider potential hazards when handling or using 14-methylcholest-7-en-3-yl acetate in various applications

Environmental impact

Information on environmental impact is not provided in the material, but it is important to consider the potential effects on the environment when using 14-methylcholest-7-en-3-yl acetate in industrial applications

Regulatory status

Information on regulatory status is not provided in the material, but it is important to consider any relevant regulations or guidelines when using 14-methylcholest-7-en-3-yl acetate in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 5259-20-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,5 and 9 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5259-20:
(6*5)+(5*2)+(4*5)+(3*9)+(2*2)+(1*0)=91
91 % 10 = 1
So 5259-20-1 is a valid CAS Registry Number.

5259-20-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name [10,13,14-trimethyl-17-(6-methylheptan-2-yl)-1,2,3,4,5,6,9,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-yl] acetate

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5259-20-1 SDS

5259-20-1Upstream product

5259-20-1Downstream Products

5259-20-1Relevant academic research and scientific papers

Chemical synthesis of three 14 alpha-hydroxymethyl cholestenols.

Pascal Jr.,Shaw,Schroepfer Jr.

, p. 570 - 578,572,573,575,576 (2007/10/13)

Reported herein are chemical syntheses of 14 alpha-hydroxymethyl-5 alpha-cholest-8-en-3 beta-ol, 14 alpha-hydroxymethyl-5 alph-cholest-7-en-3 beta-ol, and 14 alpha-hydroxymethyl-5 alpha-cholest-6-en 3 beta-ol. These compounds were obtained in pure form after repeated medium-pressure column chromatography of the mixture obtained by treatment of 3 beta-acetoxy-7 alpha,32-epoxy-14 alpha-methyl-5 alpha-cholestane with pyridine hydrochloride in refluxing acetic anhydride followed by reduction with lithium aluminum hydride. The compounds were characterized by their chromatographic properties and by the results of infrared, optical rotation, nuclear magnetic resonance, and low and high resolution mass spectral studies.

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