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1,5-Di-O-toluene-p-sulfonyl-2,3,4-tri-O-benzyl-D-arabinitol is a complex organic compound that serves as a key intermediate in the synthesis of various biologically active molecules, particularly in the field of carbohydrate chemistry. 1,5-Di-O-toluene-p-sulfonyl-2,3,4-tri-O-benzyl-D-arabinitol is characterized by its unique structure, which includes a D-arabinitol core with two toluene-p-sulfonyl groups at the 1 and 5 positions, and three benzyl groups at the 2, 3, and 4 positions. The presence of these functional groups allows for further chemical modifications and reactions, making it a valuable building block in the preparation of more complex molecules with potential applications in pharmaceuticals, agrochemicals, and other industries. The synthesis of 1,5-Di-O-toluene-p-sulfonyl-2,3,4-tri-O-benzyl-D-arabinitol typically involves multiple steps, including protection of the hydroxyl groups, sulfonylation, and benzylation, which require careful control of reaction conditions to achieve the desired product with high purity and yield.

2159-31-1

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2159-31-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2159-31-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,5 and 9 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2159-31:
(6*2)+(5*1)+(4*5)+(3*9)+(2*3)+(1*1)=71
71 % 10 = 1
So 2159-31-1 is a valid CAS Registry Number.

2159-31-1Downstream Products

2159-31-1Relevant academic research and scientific papers

Synthesis of the first pseudosugar-C-disaccharide. A potential antigen for eliciting glycoside-bond forming antibodies with catalytic groups

Barbaud,Barbaud, Christel,Bols,Bols, Mikael,Lundt,Lundt, Inge,Sierks,Sierks, Michael R.

, p. 9063 - 9078 (1995)

A number of synthetic routes to the first pseudo-C-disaccharide ever prepared has been studied. The compound, methyl-7-((1S,3R,4R,5S,6S)-1-amino-3-hydroxymethyl-4,5,6-trihydroxycyc lohexyl)-6,7-dideoxy-α-D-gluco-heptopyranoside (I), is structurally relate

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