Cas 125803-48-7,ethyl (+/-)-1,2,3,4-tetrahydro-1-methyl-2-oxo-4-phenyl-6-(1H-tetrazol-5-yl)-5-pyrimidinecarboxylate

125803-48-7

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Basic information

Product Name: ethyl (+/-)-1,2,3,4-tetrahydro-1-methyl-2-oxo-4-phenyl-6-(1H-tetrazol-5-yl)-5-pyrimidinecarboxylate
Synonyms: ethyl (+/-)-1,2,3,4-tetrahydro-1-methyl-2-oxo-4-phenyl-6-(1H-tetrazol-5-yl)-5-pyrimidinecarboxylate
CAS NO:125803-48-7
Molecular Formula:
Molecular Weight: 328.33
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: ethyl (+/-)-1,2,3,4-tetrahydro-1-methyl-2-oxo-4-phenyl-6-(1H-tetrazol-5-yl)-5-pyrimidinecarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl (+/-)-1,2,3,4-tetrahydro-1-methyl-2-oxo-4-phenyl-6-(1H-tetrazol-5-yl)-5-pyrimidinecarboxylate(125803-48-7)
EPA Substance Registry System: ethyl (+/-)-1,2,3,4-tetrahydro-1-methyl-2-oxo-4-phenyl-6-(1H-tetrazol-5-yl)-5-pyrimidinecarboxylate(125803-48-7)

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: 125803-48-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 125803-48-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,8,0 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 125803-48:
(8*1)+(7*2)+(6*5)+(5*8)+(4*0)+(3*3)+(2*4)+(1*8)=117
117 % 10 = 7
So 125803-48-7 is a valid CAS Registry Number.

125803-48-7Upstream product

125803-39-6 ethyl (+/-)-6-cyano-1,2,3,4-tetrahydro-1-methyl-2-oxo-4-phenyl-5-pyrimidinecarboxylate

125803-48-7Downstream Products

125803-48-7Relevant academic research and scientific papers

Unexpected Formation of Nitriles from Reactions of 6-(Dibromomethyl)-1,2,3,4-tetrahydro-2-oxo-5-pyrimidinearboxylates with Sodium Azide

Kappe, Oliver C.

, p. 505 - 507 (2007/10/02)

The action of sodium azide on (dibromomethyl)pyrimidines 2a and 8a leads to the nitriles 3a and 9, whereas the 1-methyl derivatives 2b and 8b afford the geminal diazides 7 and 10.The nitriles 3a,b add another mole of azide to give the tetrazoles 4a, b.The

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