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6-(S-benzyl)mercapto-1-hexanol is an organic compound with the molecular formula C13H22OS. It is a colorless liquid at room temperature and has a distinct, strong odor. This chemical is primarily used as a synthetic intermediate in the production of various pharmaceuticals, agrochemicals, and fragrances. It is characterized by its unique structure, which includes a benzyl group attached to a sulfur atom, which in turn is connected to a hexanol chain. The compound's properties, such as its reactivity and solubility, make it a valuable building block in the synthesis of complex molecules. It is also known for its potential applications in the development of new materials and chemical processes.

5755-55-5

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5755-55-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5755-55-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,5 and 5 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5755-55:
(6*5)+(5*7)+(4*5)+(3*5)+(2*5)+(1*5)=115
115 % 10 = 5
So 5755-55-5 is a valid CAS Registry Number.

5755-55-5Relevant academic research and scientific papers

Visible-Light-Driven Photocatalytic Initiation of Radical Thiol-Ene Reactions Using Bismuth Oxide

Fadeyi, Olugbeminiyi O.,Mousseau, James J.,Feng, Yiqing,Allais, Christophe,Nuhant, Philippe,Chen, Ming Z.,Pierce, Betsy,Robinson, Ralph

supporting information, p. 5756 - 5759 (2015/12/11)

A nontoxic and inexpensive photocatalytic initiation of anti-Markovnikov hydrothiolation of olefins using visible light is reported. This method is characterized by low catalyst loading, thereby enabling a mild and selective method for radical initiation in thiol-ene reactions between a wide scope of olefins and thiols.

Photocatalytic initiation of thiol-ene reactions: Synthesis of thiomorpholin-3-ones

Keylor, Mitchell H.,Park, James E.,Wallentin, Carl-Johan,Stephenson, Corey R.J.

, p. 4264 - 4269 (2014/06/09)

A mild, redox neutral photocatalytic method for alkene hydrothiolation is reported. Utilizing visible-light activation, catalytic radical initiation is achieved with the transition metal complex Ru(bpy)3Cl2, enabling rapid access to a diverse set of thiol-ene coupled products in excellent yield. On the basis of a strong observed background reaction in some cases, we have developed a solvent-free, Lewis acid-promoted tandem amidation-hydrothiolation sequence, providing thiomorpholin-3-ones in a one-pot operation from commercially available materials.

A novel one pot synthesis of benzyl sulfides: Samarium-induced, benzyl bromide mediated reduction of alkyl thiocyanates and diaryl disulfides in methanol

Zhan, Zhuang-Ping,Lang, Kai

, p. 443 - 444 (2007/10/03)

A convenient synthesis of benzyl Sulfides by the treatment of alkyl thiocyanates or diaryl disulfides with metallic samarium and benzyl bromide in methanol has been developed.

Assembly of a series of malarial glycosylphosphatidylinositol anchor oligosaccharides

Kwon, Yong-Uk,Soucy, Regina L.,Snyder, Daniel A.,Seeberger, Peter H.

, p. 2493 - 2504 (2007/10/03)

We report an efficient and convergent synthesis of a series of oligosaccharides comprised of the malaria GPI glycan (2 a), a promising anti-malaria vaccine candidate currently in preclinical trials and several related oligosaccharide sequences (3-8) that

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