Cas 343591-39-9,ethyl 4-(3,5-dibromo-4-hydroxyphenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate

343591-39-9

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Basic information

Product Name: ethyl 4-(3,5-dibromo-4-hydroxyphenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate
Synonyms:
CAS NO:343591-39-9
Molecular Formula:
Molecular Weight: 434.084
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 4-(3,5-dibromo-4-hydroxyphenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 4-(3,5-dibromo-4-hydroxyphenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate(343591-39-9)
EPA Substance Registry System: ethyl 4-(3,5-dibromo-4-hydroxyphenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate(343591-39-9)

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: 343591-39-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 343591-39-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,3,5,9 and 1 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 343591-39:
(8*3)+(7*4)+(6*3)+(5*5)+(4*9)+(3*1)+(2*3)+(1*9)=149
149 % 10 = 9
So 343591-39-9 is a valid CAS Registry Number.

343591-39-9Upstream product

343591-39-9Downstream Products

343591-39-9Relevant academic research and scientific papers

An efficient one-pot synthesis of 3,4-dihydropyrimidin-2-(1H)-ones/thiones catalysed by 2-thienylboronic acid

Fu, Zhenfang,Shen, Tianhua,Du, Zhiping,Qiao, Zhiguo,Song, Qingbao

, p. 200 - 202 (2012)

A simple efficient one-pot three-component condensation for synthesis of 3,4-dihydropyrimidin-2-(1H)-ones/thiones in good to excellent yields using 2-thienylboronic acid as a catalyst was described.

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