63598-32-3 Usage
Uses
Used in Pharmaceutical Industry:
Methyl 4,6-O-Benzylidene-2-deoxy-alpha-D-erythro-hexopyranosid-3-ulose Oxime is used as a key intermediate in the synthesis of new drugs and medications, leveraging its unique structure and properties to develop innovative pharmaceutical compounds.
Used in Organic Synthesis:
Methyl 4,6-O-Benzylidene-2-deoxy-alpha-D-erythro-hexopyranosid-3-ulose Oxime is used as a versatile building block in organic synthesis, enabling the creation of a wide range of chemical compounds with diverse applications.
Used in Chemical Research:
Methyl 4,6-O-Benzylidene-2-deoxy-alpha-D-erythro-hexopyranosid-3-ulose Oxime is used as a valuable research tool in the field of carbohydrate chemistry, contributing to the understanding of complex carbohydrate structures and their interactions with other molecules.
Used in Chemical Reactions:
Methyl 4,6-O-Benzylidene-2-deoxy-alpha-D-erythro-hexopyranosid-3-ulose Oxime is used as a reagent in various chemical reactions, facilitating the synthesis of target compounds and enhancing the efficiency of reaction processes.
Used in Laboratory Experiments:
Methyl 4,6-O-Benzylidene-2-deoxy-alpha-D-erythro-hexopyranosid-3-ulose Oxime is used as a reagent in laboratory experiments, providing researchers with a reliable and efficient tool for conducting a wide range of scientific investigations.
Check Digit Verification of cas no
The CAS Registry Mumber 63598-32-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,5,9 and 8 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 63598-32:
(7*6)+(6*3)+(5*5)+(4*9)+(3*8)+(2*3)+(1*2)=153
153 % 10 = 3
So 63598-32-3 is a valid CAS Registry Number.
InChI:InChI=1/C14H17NO5/c1-17-12-7-10(15-16)13-11(19-12)8-18-14(20-13)9-5-3-2-4-6-9/h2-6,11-14,16H,7-8H2,1H3/b15-10-/t11-,12-,13-,14?/m0/s1
63598-32-3Relevant 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
Photoaddition reactions of 3-nitro-2-enopyranoside derivatives in 1,3-dioxolane
Sakakibara,Takaide,Seta
, p. 271 - 278 (2007/10/02)
Irradiation of 3-nitro-2-enopyranoside derivatives having α-D-erythro, β-D-threo, and α-D-threo configurations in 1,3-dioxolane afforded adducts in moderate yields. Structural assignment of the adducts, including conformational analyses of the 1,3-dioxolanyl moiety, were performed. Irradiation of 3-nitro-2-enopyranoside derivatives having α-D-erythro, β-D-threo, and α-D-threo configurations in 1,3-dioxolane afforded adducts in moderate yields. Structural assignment of the adducts, including conformational analyses of the 1,3-dioxolanyl moiety, were performed.
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.
