Cas 1445609-60-8,ethyl 6-(dichloromethyl)-4-(3,4-dimethoxyphenyl)-1,2,3,4-tetrahydro-2-oxopyrimidine-5-carboxylate

1445609-60-8

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Basic information

Product Name: ethyl 6-(dichloromethyl)-4-(3,4-dimethoxyphenyl)-1,2,3,4-tetrahydro-2-oxopyrimidine-5-carboxylate
Synonyms: ethyl 6-(dichloromethyl)-4-(3,4-dimethoxyphenyl)-1,2,3,4-tetrahydro-2-oxopyrimidine-5-carboxylate
CAS NO:1445609-60-8
Molecular Formula:
Molecular Weight: 389.235
EINECS: N/A
Product Categories: N/A
Mol File: 1445609-60-8.mol
Article Data: 1

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 6-(dichloromethyl)-4-(3,4-dimethoxyphenyl)-1,2,3,4-tetrahydro-2-oxopyrimidine-5-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 6-(dichloromethyl)-4-(3,4-dimethoxyphenyl)-1,2,3,4-tetrahydro-2-oxopyrimidine-5-carboxylate(1445609-60-8)
EPA Substance Registry System: ethyl 6-(dichloromethyl)-4-(3,4-dimethoxyphenyl)-1,2,3,4-tetrahydro-2-oxopyrimidine-5-carboxylate(1445609-60-8)

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: 1445609-60-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1445609-60-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,5,6,0 and 9 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1445609-60:
(9*1)+(8*4)+(7*4)+(6*5)+(5*6)+(4*0)+(3*9)+(2*6)+(1*0)=168
168 % 10 = 8
So 1445609-60-8 is a valid CAS Registry Number.

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1445609-60-8Relevant articles and documents

Regioselective chlorination at C-6 methyl position of 3,4-dihydropyrimidin- 2(1H)-ones using (dichloroiodo)benzene

Tale, Nilesh P.,Shelke, Amol V.,Bhong, Bhagyashree Y.,Karade, Nandkishor N.

, p. 981 - 986 (2013/07/26)

The reaction of (dichloroiodo)benzene with 4-aryl-1,2,3,4-tetrahydro-6- methyl-2-oxopyrimidine-5-carboxylates and 5-acetyl-4-aryl-3,4-dihydro-6- methylpyrimidin-2(1H)-ones resulted in geminal dichlorination at the C-6 methyl position of 3,4-dihydropyrimid

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