Cas 910045-01-1,4-nitrophenyl benzyl[(2,4-dioxo-1,2,3,4-tetrahydropyrimidin-5-yl)methyl]carbamate

910045-01-1

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Basic information

Product Name: 4-nitrophenyl benzyl[(2,4-dioxo-1,2,3,4-tetrahydropyrimidin-5-yl)methyl]carbamate
Synonyms: 4-nitrophenyl benzyl[(2,4-dioxo-1,2,3,4-tetrahydropyrimidin-5-yl)methyl]carbamate
CAS NO:910045-01-1
Molecular Formula:
Molecular Weight: 396.359
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: 4-nitrophenyl benzyl[(2,4-dioxo-1,2,3,4-tetrahydropyrimidin-5-yl)methyl]carbamate(CAS DataBase Reference)
NIST Chemistry Reference: 4-nitrophenyl benzyl[(2,4-dioxo-1,2,3,4-tetrahydropyrimidin-5-yl)methyl]carbamate(910045-01-1)
EPA Substance Registry System: 4-nitrophenyl benzyl[(2,4-dioxo-1,2,3,4-tetrahydropyrimidin-5-yl)methyl]carbamate(910045-01-1)

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: 910045-01-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 910045-01-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,0,0,4 and 5 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 910045-01:
(8*9)+(7*1)+(6*0)+(5*0)+(4*4)+(3*5)+(2*0)+(1*1)=111
111 % 10 = 1
So 910045-01-1 is a valid CAS Registry Number.

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910045-01-1Relevant academic research and scientific papers

A facile synthesis of an oxazolo[5,4]pyrimidin-2-one and a pyrimido[5,4][1,3]oxazin-2-one

Dijkstra, Harmen P.,Gaulon, Catherine,Niculescu-Duvaz, Dan,Springer, Caroline J.

, p. 1519 - 1522 (2007/10/03)

A facile synthesis is reported for the construction of the five- and six-membered fused carbamate rings of an oxazolo[5,4]pyrimidin-2-one and a pyrimido[5,4][1,3]oxazin-2-one, respectively. The method utilises a controlled two-step procedure in which a re

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