Cas 1450893-68-1,N-cyclohexyl-2,3,4,5-tetrahydro-7-methyl-2,4-dioxo-1H-chromeno[2,3-d]pyrimidine-5-carboxamide

1450893-68-1

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Basic information

Product Name: N-cyclohexyl-2,3,4,5-tetrahydro-7-methyl-2,4-dioxo-1H-chromeno[2,3-d]pyrimidine-5-carboxamide
Synonyms: N-cyclohexyl-2,3,4,5-tetrahydro-7-methyl-2,4-dioxo-1H-chromeno[2,3-d]pyrimidine-5-carboxamide
CAS NO:1450893-68-1
Molecular Formula:
Molecular Weight: 355.393
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: N-cyclohexyl-2,3,4,5-tetrahydro-7-methyl-2,4-dioxo-1H-chromeno[2,3-d]pyrimidine-5-carboxamide(CAS DataBase Reference)
NIST Chemistry Reference: N-cyclohexyl-2,3,4,5-tetrahydro-7-methyl-2,4-dioxo-1H-chromeno[2,3-d]pyrimidine-5-carboxamide(1450893-68-1)
EPA Substance Registry System: N-cyclohexyl-2,3,4,5-tetrahydro-7-methyl-2,4-dioxo-1H-chromeno[2,3-d]pyrimidine-5-carboxamide(1450893-68-1)

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: 1450893-68-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1450893-68-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,0,8,9 and 3 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1450893-68:
(9*1)+(8*4)+(7*5)+(6*0)+(5*8)+(4*9)+(3*3)+(2*6)+(1*8)=181
181 % 10 = 1
So 1450893-68-1 is a valid CAS Registry Number.

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1450893-68-1Relevant academic research and scientific papers

Novel isocyanide-based three-component reaction: A facile synthesis of substituted 1H-chromeno[2,3-d]pyrimidine-5-carboxamides

Soleimani, Ebrahim,Ghorbani, Somayeh,Ghasempour, Hamid Reza

, p. 8511 - 8515 (2013)

A mild and efficient method for the synthesis of 1H-chromeno[2,3-d] pyrimidine-5-carboxamide derivatives via a one-pot, three-component reaction of an isocyanide, barbituric acid, and a salicylaldehyde in the presence of acetic acid in ethanol/water mixture at 75 C is reported. This high atom economy reaction led to the construction of one benzopyran ring, and one amide group in a single synthetic step.

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