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2,3-Seco-5β-cholestane-2,3-dioic acid dimethyl ester is a complex chemical compound derived from the metabolite of cholesterol, 2,3-seco-5β-cholestane-2,3-dioic acid. It is a dimethyl ester derivative known for its intricate molecular structure and has been a subject of study for its potential biological and pharmacological properties, particularly in the context of cholesterol metabolism and as a therapeutic target for metabolic diseases.

1180-24-1

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1180-24-1 Usage

Uses

Used in Pharmaceutical Research:
2,3-Seco-5β-cholestane-2,3-dioic acid dimethyl ester is used as a research compound for exploring its potential biological activities and pharmacological effects. It is particularly valuable in the development of new therapeutic agents targeting cholesterol metabolism and related metabolic disorders.
Used in Drug Development:
In the pharmaceutical industry, 2,3-Seco-5β-cholestane-2,3-dioic acid dimethyl ester is utilized as a lead compound in the discovery and design of novel drugs. Its unique structure and properties make it a promising candidate for the treatment of metabolic diseases, pending further research to elucidate its full potential and safety profile.

Check Digit Verification of cas no

The CAS Registry Mumber 1180-24-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,8 and 0 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1180-24:
(6*1)+(5*1)+(4*8)+(3*0)+(2*2)+(1*4)=51
51 % 10 = 1
So 1180-24-1 is a valid CAS Registry Number.

1180-24-1Relevant academic research and scientific papers

Autoxidation vs hydrolysis in 16α-acyloxy steroids

Slavikova, Barbora,Kasal, Alexander,Budesinsky, Milos

, p. 1125 - 1134 (2007/10/03)

Some enolizable α-hydroxy ketones are extremely susceptible to oxidation with traces of air in a reaction vessel. Autoxidation can be used in synthesis of oxo acids or diacids and their derivatives. Yet alkaline hydrolysis of the substrate is possible though under strictly air-free conditions.

α-nitrocycloalkanones as a source of α,ω,-dicarboxylic acid dimethyl esters

Ballini, Roberto,Bosica, Giovanna

, p. 16131 - 16138 (2007/10/03)

α,ω-Dicarboxylic acid dimethyl esters arc easily obtained by ring cleavage of α-nitrocycloalkanones. Thus, reaction of the latter compounds with three equivalents of potassium persulfate, in methanol and in presence of sulfuric acid at 80 °C, provides α,ω-dicarboxylic acid dimethyl esters in high yields. Long-chain, and alkylated α,ω-dicarboxylic acid dimethyl esters can be also efficiently obtained.

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