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S-Benzyl-β-mercaptopropionsaeure-N-hydroxysuccinimidester, also known as S-benzyl-β-mercaptopropionic acid N-hydroxysuccinimide ester (SBMP), is a chemical compound with the molecular formula C11H11NO4S. It is a white to off-white crystalline solid that is soluble in water and various organic solvents. SBMP is commonly used as a reagent in the synthesis of various organic compounds, particularly in the preparation of thiol-reactive probes and cross-linking agents. It is also employed in the modification of proteins and other biomolecules, as it can form stable thioether linkages with thiol groups present in cysteine residues. The compound is widely used in research and development, particularly in the fields of biochemistry, molecular biology, and medicinal chemistry.

3481-24-1

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3481-24-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3481-24-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,8 and 1 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3481-24:
(6*3)+(5*4)+(4*8)+(3*1)+(2*2)+(1*4)=81
81 % 10 = 1
So 3481-24-1 is a valid CAS Registry Number.

3481-24-1Downstream Products

3481-24-1Relevant academic research and scientific papers

Synthesis of some divalent O- and S-glycosides of galabiose and globotriose

Hansen, Henrik C.,Magnusson, Goeran

, p. 243 - 251 (2007/10/03)

Derivatives of galabiose (α-D-Galp-(1→4)-d-Galp) and globotriose (a- D-Galp-(1→4)-β-D-Galp(l→4)-D-Glcp) were coupled to various 1,2- and 1,3- dihydroxymethyl- and dimercaptomethylbenzenes to give the corresponding divalent glycosides, potentially useful as inhibitors of bacterial adhesion.

Di-, tri-, and tetravalent dendritic galabiosides that inhibit hemagglutination by Streptococcus suis at nanomolar concentration

Hansen, Henrik C.,Haataja, Sauli,Finne, Jukka,Magnusson, G?ran

, p. 6974 - 6979 (2007/10/03)

Galabiose (Galα1-4Gal) derivatives were coupled to carrier molecules having mono, di-, tri-, and tetrameric functionalities, thus creating mono- to tetravalent dendritic galabiosides (1-9). The di- to tetravalent galabiosides were several hundred times mo

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