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320725-47-1

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  • (2S)-2-hydroxypropanoic acid - (3beta,5alpha,7alpha,24R)-3-({3-[(4-aminobutyl)amino]propyl}amino)-7-hydroxycholestan-24-yl hydrogen sulfate (1:1)

    Cas No: 320725-47-1

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320725-47-1 Usage

General Description

The chemical compound "(2S)-2-hydroxypropanoic acid - (3beta,5alpha,7alpha,24R)-3-({3-[(4-aminobutyl)amino]propyl}amino)-7-hydroxycholestan-24-yl hydrogen sulfate (1:1)" is a complex molecule consisting of two main components. The first component is (2S)-2-hydroxypropanoic acid, which is a type of organic acid with a hydroxyl group attached to the second carbon atom. The second component is a steroid sulfate, specifically (3beta,5alpha,7alpha,24R)-3-({3-[(4-aminobutyl)amino]propyl}amino)-7-hydroxycholestan-24-yl hydrogen sulfate. (2S)-2-hydroxypropanoic acid - (3beta,5alpha,7alpha,24R)-3-({3-[(4-aminobutyl)amino]propyl}amino)-7-hydroxycholestan-24-yl hydrogen sulfate (1:1) is a derivative of cholesterol, with a sulfate group attached to the hydroxyl group at the 24th carbon atom. The overall compound is formed by the combination of these two components in a 1:1 ratio, resulting in a complex molecule with specific stereochemistry and functional groups.

Check Digit Verification of cas no

The CAS Registry Mumber 320725-47-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,0,7,2 and 5 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 320725-47:
(8*3)+(7*2)+(6*0)+(5*7)+(4*2)+(3*5)+(2*4)+(1*7)=111
111 % 10 = 1
So 320725-47-1 is a valid CAS Registry Number.

320725-47-1Downstream Products

320725-47-1Relevant articles and documents

CRYSTALLINE FORMS OF SQUALAMINE

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, (2021/09/26)

This disclosure provides crystalline polymorphs of squalamine phosphate, methods of making the same, and methods of treatment using the same.

Polymorphic and amorphous salt forms of squalamine dilactate

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Page/Page column 10-11, (2010/11/25)

The invention relates to select squalamine salts, methods of their synthesis, their therapeutic use and their advantages relating to manufacturing, product stability and toxicity. More specifically, this application is directed to various forms of the dil

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