Cas 1158951-44-0,(2R,5R)-2-(3-((benzyloxy)methyl)-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-5-(hydroxymethyl)-4-methoxytetrahydrofuran-3-yl acetate

1158951-44-0

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Basic information

Product Name: (2R,5R)-2-(3-((benzyloxy)methyl)-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-5-(hydroxymethyl)-4-methoxytetrahydrofuran-3-yl acetate
Synonyms: (2R,5R)-2-(3-((benzyloxy)methyl)-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-5-(hydroxymethyl)-4-methoxytetrahydrofuran-3-yl acetate
CAS NO:1158951-44-0
Molecular Formula:
Molecular Weight: 420.419
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (2R,5R)-2-(3-((benzyloxy)methyl)-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-5-(hydroxymethyl)-4-methoxytetrahydrofuran-3-yl acetate(CAS DataBase Reference)
NIST Chemistry Reference: (2R,5R)-2-(3-((benzyloxy)methyl)-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-5-(hydroxymethyl)-4-methoxytetrahydrofuran-3-yl acetate(1158951-44-0)
EPA Substance Registry System: (2R,5R)-2-(3-((benzyloxy)methyl)-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-5-(hydroxymethyl)-4-methoxytetrahydrofuran-3-yl acetate(1158951-44-0)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1158951-44-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1158951-44-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,5,8,9,5 and 1 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1158951-44:
(9*1)+(8*1)+(7*5)+(6*8)+(5*9)+(4*5)+(3*1)+(2*4)+(1*4)=180
180 % 10 = 0
So 1158951-44-0 is a valid CAS Registry Number.

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1158951-44-0Relevant academic research and scientific papers

Concise synthesis of capuramycin

Kurosu, Michio,Li, Kai,Crick, Dean C.

, p. 2393 - 2396 (2009)

A concise total synthesis of capuramycin (1), a promising preclinical TB drug lead, is achieved by high-yield formations of the cyanohydrin 5a and 4″,5″-glycal derivative 12. Capuramycin can be synthesized in eight steps from the uridine building block 5a with 30% overall yield. The synthetic intermediates reported here are useful for generation of analogs to improve pharmacokinetic properties of capuramycin.

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