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methyl 7α-methoxymethyloxy-3-oxo-5β-cholan-24-oate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

610313-89-8

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610313-89-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 610313-89-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,1,0,3,1 and 3 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 610313-89:
(8*6)+(7*1)+(6*0)+(5*3)+(4*1)+(3*3)+(2*8)+(1*9)=108
108 % 10 = 8
So 610313-89-8 is a valid CAS Registry Number.

610313-89-8Relevant academic research and scientific papers

METHOD AND COMPOSITIONS FOR FORMING A COPPER-CONTAINING COMPLEX AND USES THEREOF

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Paragraph 0156, (2019/05/22)

Provided is a method of forming a copper-containing complex, including contacting a sample containing copper with a compound of Formula (I): wherein R is -OH or -O-CH3. Also provided is a method of inhibiting enzymatic activity of a kinase in a sample, including contacting the sample with a compound of Formula (I). Further provided is a method of administering to a subject a pharmaceutical composition including a compound of Formula (I) optionally complexed with copper. Also provided is a pharmaceutical composition including copper complexed with a compound of Formula (I).

A stereoselective synthesis of the allo-bile acids from the 5β-isomers

Li, Qingjiang,Tochtrop, Gregory P.

supporting information; experimental part, p. 4137 - 4139 (2011/09/19)

The allo-bile acids are a subset of the family of steroidal detergents found in most vertebrates. Because there are no major biological feedstocks for isolation of the allo-bile acids, they must be synthesized from the abundant 5β-reduced isomers. Here we report a general set of methods for the synthesis of allo-bile acids from the corresponding 5-β isomers demarcated by a selective C-3 oxidation, IBX unsaturation, and stereoselective saturation.

A concise and stereoselective synthesis of squalamine

Zhang, Dong-Hui,Cai, Feng,Zhou, Xiang-Dong,Zhou, Wei-Shan

, p. 3257 - 3259 (2007/10/03)

(Matrix presented) A short and highly stereoselective synthesis of the novel steroid squalamine (1) was accomplished in nine steps from easily available methyl chenodeoxylcholanate 2. Our synthesis featured improved dehydrogenation of 4 followed by conjugate reduction to construct the trans AB-ring system and efficient asymmetric isopropylation of aldehyde 6 to introduce the C-24R-hydroxyl group.

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