Cas 1415409-81-2,2',3',5'-tri-O-acetyl-3-[(2Z)-4-(adamantan-1-ylamino)-3-(3-chloro-4-fluorophenyl)but-2-en-1-yl]uridine

1415409-81-2

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Basic information

Product Name: 2',3',5'-tri-O-acetyl-3-[(2Z)-4-(adamantan-1-ylamino)-3-(3-chloro-4-fluorophenyl)but-2-en-1-yl]uridine
Synonyms: 2',3',5'-tri-O-acetyl-3-[(2Z)-4-(adamantan-1-ylamino)-3-(3-chloro-4-fluorophenyl)but-2-en-1-yl]uridine
CAS NO:1415409-81-2
Molecular Formula:
Molecular Weight: 702.177
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',3',5'-tri-O-acetyl-3-[(2Z)-4-(adamantan-1-ylamino)-3-(3-chloro-4-fluorophenyl)but-2-en-1-yl]uridine(CAS DataBase Reference)
NIST Chemistry Reference: 2',3',5'-tri-O-acetyl-3-[(2Z)-4-(adamantan-1-ylamino)-3-(3-chloro-4-fluorophenyl)but-2-en-1-yl]uridine(1415409-81-2)
EPA Substance Registry System: 2',3',5'-tri-O-acetyl-3-[(2Z)-4-(adamantan-1-ylamino)-3-(3-chloro-4-fluorophenyl)but-2-en-1-yl]uridine(1415409-81-2)

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: 1415409-81-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1415409-81-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,5,4,0 and 9 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1415409-81:
(9*1)+(8*4)+(7*1)+(6*5)+(5*4)+(4*0)+(3*9)+(2*8)+(1*1)=142
142 % 10 = 2
So 1415409-81-2 is a valid CAS Registry Number.

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1415409-81-2Relevant academic research and scientific papers

Exploiting adamantane as a versatile organic tecton: Multicomponent catalytic cascade reactions

Grigg, Ronald,Elboray, Elghareeb E.,Aly, Moustafa F.,Abbas-Temirek, Hussien H.

, p. 11504 - 11506,3 (2012)

3- And 9-component Pd(0) catalysed assembly of allenes, aryl iodides and N-nucleophiles with concomitant installation of trisubstituted Z-alkenes is readily achieved. This journal is

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