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N-{(1-hydroxycyclohexyl)methyl}-4-methylbenzenesulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

58107-53-2

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58107-53-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58107-53-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,1,0 and 7 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 58107-53:
(7*5)+(6*8)+(5*1)+(4*0)+(3*7)+(2*5)+(1*3)=122
122 % 10 = 2
So 58107-53-2 is a valid CAS Registry Number.

58107-53-2Relevant academic research and scientific papers

A One-Pot Reaction toward the Diastereoselective Synthesis of Substituted Morpholines

Aubineau, Thomas,Cossy, Janine

, p. 7419 - 7423 (2018/12/11)

The diastereoselective synthesis of various substituted morpholines has been achieved from vinyloxiranes and amino-alcohols under sequential Pd(0)-catalyzed Tsuji-Trost/Fe(III)-catalyzed heterocyclization. Using the same strategy, 2,6-, 2,5-, and 2,3-disubstituted as well as 2,5,6- and 2,3,5-trisubstituted morpholines were obtained in good to excellent yields and diastereoselectivities.

Synthesis of 1,2-amino alcohols via catalytic C-H amidation of sp3 methyl C-H bonds

Kang, Taek,Kim, Heejeong,Kim, Jeung Gon,Chang, Sukbok

supporting information, p. 12073 - 12075 (2014/12/11)

Herein a new synthetic route to 1,2-amino alcohols is presented by using C-H amidation of sp3 methyl C-H bonds as a key step. Readily available alcohols were employed as starting materials after converting them to removable ketoxime chelating g

Gold-catalyzed direct activation of allylic alcohols in the stereoselective synthesis of functionalized 2-vinyl-morpholines

Bandini, Marco,Monari, Magda,Romaniello, Alessandro,Tragni, Michele

supporting information; body text, p. 14272 - 14277 (2011/03/19)

Alcohol versus alcohol: A highly stereocontrolled synthesis of substituted morpholines is realized by means of gold-catalyzed dehydrative allylic cyclization of diols (see scheme for one example; segphos = 5,5′-bis[di(3, 5-di-tert-butyl-4-methyoxyphenyl)phosphine]-4,4′-bi-1,3-benzodioxole). The present methodology represents one of the few examples of enantioselective gold-catalyzed transformations involving unactivated alkenes. Copyright

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