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Benzenemethanol, 2-(mercaptomethyl)-, also known as 2-(mercaptomethyl)benzenemethanol or 2-(hydroxymethyl)benzenemethanethiol, is an organic compound with the chemical formula C8H10OS. It is a colorless to pale yellow liquid with a molecular weight of 154.23 g/mol. Benzenemethanol, 2-(mercaptomethyl)- is characterized by the presence of a benzene ring, a hydroxymethyl group, and a thiol (mercapto) group. It is used in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds due to its unique chemical properties. The compound is sensitive to air and moisture, and it is typically stored under an inert atmosphere to prevent oxidation and degradation.

26257-08-9

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26257-08-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26257-08-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,2,5 and 7 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 26257-08:
(7*2)+(6*6)+(5*2)+(4*5)+(3*7)+(2*0)+(1*8)=109
109 % 10 = 9
So 26257-08-9 is a valid CAS Registry Number.

26257-08-9Relevant academic research and scientific papers

Next-Generation Reduction Sensitive Lipid Conjugates of Tenofovir: Antiviral Activity and Mechanism of Release

Giesler, Kyle E.,Liotta, Dennis C.

, p. 10244 - 10252 (2016)

The pharmacokinetic properties of tenofovir (TFV) and other charged nucleoside analogues are dramatically improved upon conjugation to a lipid prodrug. We previously prepared reduction-sensitive lipid conjugates of TFV that demonstrate superior antiviral

POLYNUCLEOTIDE CONSTRUCTS HAVING DISULFIDE GROUPS

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Page/Page column 91, (2015/05/26)

The invention features polynucleotide constructs containing one or more components (i) containing a disulfide linkage, where each of the one or more components is attached to an internudeotide bridging group or a terminal group of the polynucleotide construct, and each of the one or more components (i) contains one or more bulky groups proximal to the disulfide group. The invention also features polynucleotide constructs containing one or more components (i) containing a disulfide linkage, where each of the one or more components (i) is attached to an internudeotide bridging group or a terminal group of the polynucleotide construct, and each of the one or more components (i) contains at least 4 atoms in a chain between the disulfide linkage and the phosphorus atom of the internudeotide bridging group or the terminal group; and where the chain does not contain a phosphate, an amide, an ester, or an alkenylene. The invention also features methods of delivering a polynucleotide to a cell using the polynucleotide constructs of the invention.

POLYNUCLEOTIDE CONSTRUCTS HAVING BIOREVERSIBLE AND NON-BIOREVERSIBLE GROUPS

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Page/Page column 79, (2016/02/19)

The invention features a hybridized polynucleotide construct containing a passenger strand, a guide strand loadable into a RISC complex, and (i) a 3'-terminal or an internucleotide non-bioreversible group in the guide strand; or (ii) a 5'-terminal, a 3'-terminal, or an internucleotide non-bioreversible group in the passenger strand, and a 5'-terminal, a 3'-terminal, or an internucleotide disulfide bioreversible group in the guide strand or the passenger strand. The invention also features methods of delivering a polynucleotide to a cell using the hybridized polynucleotide construct. The invention further features methods of reducing the expression of a polypeptide in a cell using the hybridized polynucleotide construct.

AN EASY PREPARATION OF SIMPLE SULTINES AND HYDROXYALKANESULFINATE SALTS

King, J. F.,Rathore, Rajenda

, p. 2763 - 2766 (2007/10/02)

In accord with mechanistic prediction a one-pot, two-stage, controlled chlorination-hydrolysis of HO(CH2)nSH gave the sultine when n=3 or 4, and the polymeric sulfinic ester when n=5 or 6; alkaline hydrolysis of either product yielded the corresponding sodium ω-hydroxy-1-alkanesulfinate.

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