Cas 1228425-04-4,2-(4,5-dihydroxy-2-methylphenyl)-1-phenyl-2-(tetrahydropyrimidin-2(1H)-ylidene)ethanone

1228425-04-4

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Basic information

Product Name: 2-(4,5-dihydroxy-2-methylphenyl)-1-phenyl-2-(tetrahydropyrimidin-2(1H)-ylidene)ethanone
Synonyms:
CAS NO:1228425-04-4
Molecular Formula:
Molecular Weight: 324.379
EINECS: N/A
Product Categories: N/A
Mol File: 1228425-04-4.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: 2-(4,5-dihydroxy-2-methylphenyl)-1-phenyl-2-(tetrahydropyrimidin-2(1H)-ylidene)ethanone(CAS DataBase Reference)
NIST Chemistry Reference: 2-(4,5-dihydroxy-2-methylphenyl)-1-phenyl-2-(tetrahydropyrimidin-2(1H)-ylidene)ethanone(1228425-04-4)
EPA Substance Registry System: 2-(4,5-dihydroxy-2-methylphenyl)-1-phenyl-2-(tetrahydropyrimidin-2(1H)-ylidene)ethanone(1228425-04-4)

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: 1228425-04-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1228425-04-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,8,4,2 and 5 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1228425-04:
(9*1)+(8*2)+(7*2)+(6*8)+(5*4)+(4*2)+(3*5)+(2*0)+(1*4)=134
134 % 10 = 4
So 1228425-04-4 is a valid CAS Registry Number.

1228425-04-4Upstream product

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1228425-04-4Relevant articles and documents

Anodic oxidation of catechols in the presence of α-oxoketene N,N-acetals with a tetrahydropyrimidine ring: Selective α-arylation reaction

Zeng, Cheng-Chu,Ping, Da-Wei,Hu, Li-Ming,Song, Xiu-Qing,Zhong, Ru-Gang

experimental part, p. 2465 - 2472 (2010/07/06)

The electrochemical oxidation of catechols leads to the formation of o-benzoquinones. This property has been applied to effectively synthesize α-arylated products of α-oxoketene N,N-acetals with a tetrahydropyrimidine ring.

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