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2-(benzyloxycarbonylamino)-2-deoxy-3,4:5,6-di-O-isopropylidene-aldehydo-D-glucose dimethyl acetal is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73707-67-2

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73707-67-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73707-67-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,7,0 and 7 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 73707-67:
(7*7)+(6*3)+(5*7)+(4*0)+(3*7)+(2*6)+(1*7)=142
142 % 10 = 2
So 73707-67-2 is a valid CAS Registry Number.

73707-67-2Relevant academic research and scientific papers

D-Glucosamine propanedithioacetal, an efficient chiral auxiliary in β-lactam chemistry

Anaya, Josefa,Gero, Stephane D.,Grande, Manuel,Hernando, Jose Ignacio M.,Laso, Nieves M.

, p. 837 - 850 (2007/10/03)

The synthesis of some monocyclic β-lactams (monobactams) by the Staudinger reaction using d-glucosamine propanedithioacetal as chiral auxiliary is reported. The influence of several radicals at C3, C4, and C(1') (sugar moiety) as well as other structural aspects are considered in relation to the antielastase activity. Copyright (C) 1999 Elsevier Science Ltd.

ONE-FLASK SYNTHESIS OF TRIACETALATED ALDOHEXOSES WITH 2,2-DIALKOXYPROPANE AND P-TOLUENESULFONIC ACID

Kiso, Makoto,Kondo, Akihiro,Kondo, Yumi,Hasegawa, Akira

, p. 121 - 128 (2007/10/02)

2-Deoxy-D-arabino-hexose and some N-protected 2-amino-2-deoxy-D-glucose derivatives were each treated with 2,2-dimethoxy- or 2,2-dibenzyloxy-propane in 1,4-dioxane in the presence of p-toluenesulfonic acid at 60-70 deg.The major products were acyclic, dim

A SIMPLE PREPARATION OF 2-(ACYLAMINO)-2-DEOXY-3,4:5,6-DI-O-ISOPROPYLIDENE-aldehydo-D-GLUCOSE DIMETHYL AND DIBENZYL ACETAL

Hasegawa, Akira,Kiso, Makoto

, p. 265 - 270 (2007/10/02)

When treated with a large excess of 2,2-dimethoxypropane or 2,2-dibenzyloxypropane in 1,4-dioxane solution in the presence of p-toluenesulfonic acid, 2-acetamido-2-deoxy-D-glucose and 2-(benzyloxycarbonylamino)-2-deoxy-D-glucose yield the corresponding 3,4:5,6-di-O-isopropylidene-aldehydo-D-glucose dimethyl or dibenzyl acetal in good yield.

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