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methyl 4,6-O-benzylidene-2-deoxy-3-oximino-β-D-erythro-hexopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

139757-39-4

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139757-39-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 139757-39-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,7,5 and 7 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 139757-39:
(8*1)+(7*3)+(6*9)+(5*7)+(4*5)+(3*7)+(2*3)+(1*9)=174
174 % 10 = 4
So 139757-39-4 is a valid CAS Registry Number.

139757-39-4Relevant academic research and scientific papers

Experimental and Theoretical (AM1) Studies on Photoaddition Reactions of 3-Nitro-2-enopyranoside Derivatives

Sakakibara, Tohru,Matuo, Ichiro,Takaide, Aya,Nakamura, Takanori,Seta, Akinori

, p. 177 - 180 (2007/10/02)

Irradiation of 3-nitro-α- and β-D-erythro-hex-2-enopyranoside derivatives in methanol, ethanol, and isopropanol with high pressure Hg lamp gave the adducts in moderate yields.The stereoselectivities calculated by AM1 calculation by the use of model compou

A PRACTICABLE SYNTHESIS OF N-TRIFLUOROACETYL-L-DAUNOSAMINE FROM D-GlUCOSE

Crugnola, Angelo,Lombardi, Paolo,Gandolfi, Carmelo,Arcamone, Federico

, p. 395 - 400 (2007/10/02)

A synthesis of the N-trifluoroacetyl derivative of L-daunosamine, the glucidic component of adriamycin and daunomycin, two antibiotics with proved antineoplastic activity, is described starting from D-glucose, an inexpensive carbohydrate source.The synthetic sequence involves the stereoselective introduction of the C(3) amino group and the inversion at C(5), obtained by the stereospecific hydrogenation of a 5-methylenepyranose derivative, to flip from the D over the L series.

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