153165-72-1 Usage
General Description
"(R)-Tetrahydro-2-furancarbothioic acid" is a chemical compound widely employed in the field of organic synthesis. It is a stereoisomer, specifically a derivative of tetrahydrofuran, with an added carbothioic acid group. (R)-Tetrahydro-2-furancarbothioic acid has important uses in various research and industrial areas due to its molecular structure and reactive properties. It forms part of a group of sulfur-containing organic compounds which are of significant interest for their potential medicinal uses and role in complex syntheses. Due to its specific arrangement of atoms, it displays unique chemical behaviour. The compound isn't widely available and is often custom synthesized for specific research purposes.
Check Digit Verification of cas no
The CAS Registry Mumber 153165-72-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,1,6 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 153165-72:
(8*1)+(7*5)+(6*3)+(5*1)+(4*6)+(3*5)+(2*7)+(1*2)=121
121 % 10 = 1
So 153165-72-1 is a valid CAS Registry Number.
153165-72-1Relevant articles and documents
R-(+)-thio tetrahydrofuran-2-carboxylic acid synthesis method
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Paragraph 0046; 0047, (2017/01/26)
The invention belongs to the field of pharmaceutical chemicals and particularly relates to a synthetic method of R-(+)-sulfotetrahydrofuran-2-formic acid. The method solves the technical problem that the existing method is more in reaction steps and low in cost, needs high-toxicity and high-danger raw materials and is not environmentally friendly. The technical scheme solving the technical problem is that the invention provides the synthetic method of R-(+)-sulfotetrahydrofuran-2-formic acid which comprises the following steps: dissolving R-(+)-tetrahydrofuran-2-formic acid in an organic solvent; and then adding hydrogenated xanthogen and an organic alkali to react to obtain the R-(+)-sulfotetrahydrofuran-2-formic acid. The method is few in reaction step, free from high-toxicity and high-danger raw materials and environmentally friendly, and the yield is improved.
