Cas 1033726-46-3,benzyl 3-tert-butyloxycarbonyl-(tetrahydro)pyrimidin-2-one-4(S)-carboxylate

1033726-46-3

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Basic information

Product Name: benzyl 3-tert-butyloxycarbonyl-(tetrahydro)pyrimidin-2-one-4(S)-carboxylate
Synonyms: benzyl 3-tert-butyloxycarbonyl-(tetrahydro)pyrimidin-2-one-4(S)-carboxylate
CAS NO:1033726-46-3
Molecular Formula:
Molecular Weight: 334.372
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: benzyl 3-tert-butyloxycarbonyl-(tetrahydro)pyrimidin-2-one-4(S)-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: benzyl 3-tert-butyloxycarbonyl-(tetrahydro)pyrimidin-2-one-4(S)-carboxylate(1033726-46-3)
EPA Substance Registry System: benzyl 3-tert-butyloxycarbonyl-(tetrahydro)pyrimidin-2-one-4(S)-carboxylate(1033726-46-3)

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: 1033726-46-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1033726-46-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,3,7,2 and 6 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1033726-46:
(9*1)+(8*0)+(7*3)+(6*3)+(5*7)+(4*2)+(3*6)+(2*4)+(1*6)=123
123 % 10 = 3
So 1033726-46-3 is a valid CAS Registry Number.

1033726-46-3Upstream product

61543-21-3 (S)-benzyl 5-amino-2-((tert-butoxycarbonyl)amino)-5-oxopentanoate

1033726-46-3Downstream Products

1033726-46-3Relevant academic research and scientific papers

Synthesis of imidazolidin-2-one-4-carboxylate and of (tetrahydro)pyrimidin- 2-one-5-carboxylate via an efficient modification of the Hofmann rearrangement

Angelici, Gaetano,Contaldi, Simone,Lynn Green, Sarah,Tomasini, Claudia

, p. 1849 - 1852 (2008)

A mild and efficient methodology for the rearrangement of protected asparagine and protected glutamine is reported; good results are obtained with a wide selection of protecting groups. The Royal Society of Chemistry.

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