Cas 1379463-55-4,N-cyclohexyl-2-ethyl-2-(N-ethyl-2-((6-oxo-4-propyl-1,6-dihydropyrimidin-2-yl)thio)acetamido)butanamide

1379463-55-4

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Basic information

Product Name: N-cyclohexyl-2-ethyl-2-(N-ethyl-2-((6-oxo-4-propyl-1,6-dihydropyrimidin-2-yl)thio)acetamido)butanamide
Synonyms:
CAS NO:1379463-55-4
Molecular Formula:
Molecular Weight: 450.646
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-ethyl-2-(N-ethyl-2-((6-oxo-4-propyl-1,6-dihydropyrimidin-2-yl)thio)acetamido)butanamide(CAS DataBase Reference)
NIST Chemistry Reference: N-cyclohexyl-2-ethyl-2-(N-ethyl-2-((6-oxo-4-propyl-1,6-dihydropyrimidin-2-yl)thio)acetamido)butanamide(1379463-55-4)
EPA Substance Registry System: N-cyclohexyl-2-ethyl-2-(N-ethyl-2-((6-oxo-4-propyl-1,6-dihydropyrimidin-2-yl)thio)acetamido)butanamide(1379463-55-4)

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: 1379463-55-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1379463-55-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,9,4,6 and 3 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1379463-55:
(9*1)+(8*3)+(7*7)+(6*9)+(5*4)+(4*6)+(3*3)+(2*5)+(1*5)=204
204 % 10 = 4
So 1379463-55-4 is a valid CAS Registry Number.

1379463-55-4Upstream product

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1379463-55-4Relevant academic research and scientific papers

Efficient synthesis of S-dipeptidothiouracil derivatives via a one-pot, five-component reaction under ionic liquid condition

Shahvelayati, Ashraf Sadat,Esmaeeli, Zohreh

experimental part, p. 319 - 325 (2012/08/28)

S-Dipeptidothiouracil derivatives were successfully synthesized via a one-pot, five-component nucleophilic addition/Ugi reaction sequence under ionic liquid conditions at room temperature. Simplicity, green condition, and high yields of products are advantages of this method.

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