Cas 88727-89-3,1-{1-[2-(2-Methoxy-phenyl)-pyrimidin-4-yl]-5-methyl-1H-[1,2,3]triazol-4-yl}-ethanone

88727-89-3

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Basic information

Product Name: 1-{1-[2-(2-Methoxy-phenyl)-pyrimidin-4-yl]-5-methyl-1H-[1,2,3]triazol-4-yl}-ethanone
Synonyms: 1-{1-[2-(2-Methoxy-phenyl)-pyrimidin-4-yl]-5-methyl-1H-[1,2,3]triazol-4-yl}-ethanone
CAS NO:88727-89-3
Molecular Formula:
Molecular Weight: 309.327
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: 1-{1-[2-(2-Methoxy-phenyl)-pyrimidin-4-yl]-5-methyl-1H-[1,2,3]triazol-4-yl}-ethanone(CAS DataBase Reference)
NIST Chemistry Reference: 1-{1-[2-(2-Methoxy-phenyl)-pyrimidin-4-yl]-5-methyl-1H-[1,2,3]triazol-4-yl}-ethanone(88727-89-3)
EPA Substance Registry System: 1-{1-[2-(2-Methoxy-phenyl)-pyrimidin-4-yl]-5-methyl-1H-[1,2,3]triazol-4-yl}-ethanone(88727-89-3)

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: 88727-89-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 88727-89-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,7,2 and 7 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 88727-89:
(7*8)+(6*8)+(5*7)+(4*2)+(3*7)+(2*8)+(1*9)=193
193 % 10 = 3
So 88727-89-3 is a valid CAS Registry Number.

88727-89-3Upstream product

88727-89-3Downstream Products

88727-89-3Relevant academic research and scientific papers

Reaction of Aryl-Substituted Azidopyrimidines with 1,3-Dicarbonyl Compounds

Krivopalov, V. P.,Nikolaenkova, E. B.,Sedova, V. F.,Mamaev, V. P.

, p. 1116 - 1119 (2007/10/02)

Substituted 1-pyrimidyl-4-acyl-1,2,3-triazoles were obtained by the reaction of 2- and 4-azidopyrimidines with aryl substituents with acetyl- or benzoylacetone.An accelerating effect of an o-hydroxyphenylpyrimidine fragment in this reaction, which was explained by the effect of an intramolecular hydrogen bond, was observed.

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