Cas 1296205-12-3,ethyl 1-(ethoxymethyl)-6-(4-fluorophenyl)-4-methyl-2-oxo-1,2,3,6-tetrahydropyrimidine-5-carboxylate

1296205-12-3

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Basic information

Product Name: ethyl 1-(ethoxymethyl)-6-(4-fluorophenyl)-4-methyl-2-oxo-1,2,3,6-tetrahydropyrimidine-5-carboxylate
Synonyms: ethyl 1-(ethoxymethyl)-6-(4-fluorophenyl)-4-methyl-2-oxo-1,2,3,6-tetrahydropyrimidine-5-carboxylate
CAS NO:1296205-12-3
Molecular Formula:
Molecular Weight: 336.363
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-(ethoxymethyl)-6-(4-fluorophenyl)-4-methyl-2-oxo-1,2,3,6-tetrahydropyrimidine-5-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 1-(ethoxymethyl)-6-(4-fluorophenyl)-4-methyl-2-oxo-1,2,3,6-tetrahydropyrimidine-5-carboxylate(1296205-12-3)
EPA Substance Registry System: ethyl 1-(ethoxymethyl)-6-(4-fluorophenyl)-4-methyl-2-oxo-1,2,3,6-tetrahydropyrimidine-5-carboxylate(1296205-12-3)

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: 1296205-12-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1296205-12-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,9,6,2,0 and 5 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1296205-12:
(9*1)+(8*2)+(7*9)+(6*6)+(5*2)+(4*0)+(3*5)+(2*1)+(1*2)=153
153 % 10 = 3
So 1296205-12-3 is a valid CAS Registry Number.

1296205-12-3Upstream product

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1296205-12-3Relevant academic research and scientific papers

N-Alkoxymethylation of heterocyclic compounds with diethyl phosphite via cleavage of P-O bond

Quan, Zheng-Jun,Ren, Rong-Guo,Jia, Xiao-Dong,Da, Yu-Xia,Zhang, Zhang,Wang, Xi-Cun

experimental part, p. 2462 - 2467 (2011/04/26)

N-Alkoxymethylation of heterocyclic compounds with diethyl phosphite via cleavage of P-O bond was investigated and a series of N3-ethoxymethylated heterocyclic compounds were synthesized. A mechanism in which diethyl phosphite acts as an efficient surrogate of ethanol was proposed and supported by several evidences.

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