Cas 130001-07-9,5-(4-Methoxy-phenyl)-7-methyl-2-thioxo-1,2,3,5-tetrahydro-pyrano[2,3-d]pyrimidin-4-one

130001-07-9

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Basic information

Product Name: 5-(4-Methoxy-phenyl)-7-methyl-2-thioxo-1,2,3,5-tetrahydro-pyrano[2,3-d]pyrimidin-4-one
Synonyms: 5-(4-Methoxy-phenyl)-7-methyl-2-thioxo-1,2,3,5-tetrahydro-pyrano[2,3-d]pyrimidin-4-one
CAS NO:130001-07-9
Molecular Formula:
Molecular Weight: 302.354
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: 5-(4-Methoxy-phenyl)-7-methyl-2-thioxo-1,2,3,5-tetrahydro-pyrano[2,3-d]pyrimidin-4-one(CAS DataBase Reference)
NIST Chemistry Reference: 5-(4-Methoxy-phenyl)-7-methyl-2-thioxo-1,2,3,5-tetrahydro-pyrano[2,3-d]pyrimidin-4-one(130001-07-9)
EPA Substance Registry System: 5-(4-Methoxy-phenyl)-7-methyl-2-thioxo-1,2,3,5-tetrahydro-pyrano[2,3-d]pyrimidin-4-one(130001-07-9)

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: 130001-07-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 130001-07-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,0,0 and 1 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 130001-07:
(8*1)+(7*3)+(6*0)+(5*0)+(4*0)+(3*1)+(2*0)+(1*7)=39
39 % 10 = 9
So 130001-07-9 is a valid CAS Registry Number.

130001-07-9Upstream product

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130001-07-9Relevant academic research and scientific papers

A Convenient One Pot Synthesis of 1,3,5-Triaryl-1,2,3,4-tetrahydro-4-oxo-7-methyl-2-thioxo-5H-pyranopyrimidines

Ahluwalia, V.K.,Kumar, Rakesh,Alauddin, M.,Khanduri, C.H.,Mallika, N.

, p. 1265 - 1272 (2007/10/02)

A convenient one pot synthesis of 1,3,5-triaryl-1,2,3,4-tetrahydro-4-oxo-7-methyl-2-thioxo-5H-pyranopyrimidines (1a-y) has been achived by the condensation of different 2-thiobarbituric acids (2a-h) with benzylideneacetones (3a-d) in glacial acetic

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