Cas 1379463-50-9,2-(N-benzyl-2-((6-oxo-4-propyl-1,6-dihydropyrimidin-2-yl)thio)acetamido)-N-cyclohexyl-2-ethylbutanamide

1379463-50-9

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Basic information

Product Name: 2-(N-benzyl-2-((6-oxo-4-propyl-1,6-dihydropyrimidin-2-yl)thio)acetamido)-N-cyclohexyl-2-ethylbutanamide
Synonyms:
CAS NO:1379463-50-9
Molecular Formula:
Molecular Weight: 512.717
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: 2-(N-benzyl-2-((6-oxo-4-propyl-1,6-dihydropyrimidin-2-yl)thio)acetamido)-N-cyclohexyl-2-ethylbutanamide(CAS DataBase Reference)
NIST Chemistry Reference: 2-(N-benzyl-2-((6-oxo-4-propyl-1,6-dihydropyrimidin-2-yl)thio)acetamido)-N-cyclohexyl-2-ethylbutanamide(1379463-50-9)
EPA Substance Registry System: 2-(N-benzyl-2-((6-oxo-4-propyl-1,6-dihydropyrimidin-2-yl)thio)acetamido)-N-cyclohexyl-2-ethylbutanamide(1379463-50-9)

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: 1379463-50-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1379463-50-9 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 0 respectively.
Calculate Digit Verification of CAS Registry Number 1379463-50:
(9*1)+(8*3)+(7*7)+(6*9)+(5*4)+(4*6)+(3*3)+(2*5)+(1*0)=199
199 % 10 = 9
So 1379463-50-9 is a valid CAS Registry Number.

1379463-50-9Upstream product

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1379463-50-9Relevant 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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