Cas 1403611-80-2,(2R,3R,4R,5R)-2-(acetoxymethyl)-5-(2,6-dichloro-8-cyclohexyl-9H-purin-9-yl)tetrahydrofuran-3,4-diyl diacetate

1403611-80-2

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Basic information

Product Name: (2R,3R,4R,5R)-2-(acetoxymethyl)-5-(2,6-dichloro-8-cyclohexyl-9H-purin-9-yl)tetrahydrofuran-3,4-diyl diacetate
Synonyms: (2R,3R,4R,5R)-2-(acetoxymethyl)-5-(2,6-dichloro-8-cyclohexyl-9H-purin-9-yl)tetrahydrofuran-3,4-diyl diacetate
CAS NO:1403611-80-2
Molecular Formula:
Molecular Weight: 529.377
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: (2R,3R,4R,5R)-2-(acetoxymethyl)-5-(2,6-dichloro-8-cyclohexyl-9H-purin-9-yl)tetrahydrofuran-3,4-diyl diacetate(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3R,4R,5R)-2-(acetoxymethyl)-5-(2,6-dichloro-8-cyclohexyl-9H-purin-9-yl)tetrahydrofuran-3,4-diyl diacetate(1403611-80-2)
EPA Substance Registry System: (2R,3R,4R,5R)-2-(acetoxymethyl)-5-(2,6-dichloro-8-cyclohexyl-9H-purin-9-yl)tetrahydrofuran-3,4-diyl diacetate(1403611-80-2)

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: 1403611-80-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1403611-80-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,3,6,1 and 1 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1403611-80:
(9*1)+(8*4)+(7*0)+(6*3)+(5*6)+(4*1)+(3*1)+(2*8)+(1*0)=112
112 % 10 = 2
So 1403611-80-2 is a valid CAS Registry Number.

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1403611-80-2Relevant academic research and scientific papers

CuI controlled C-C and C-N bond formation of heteroaromatics through C(sp3)-H activation

Xia, Ran,Niu, Hong-Ying,Qu, Gui-Rong,Guo, Hai-Ming

, p. 5546 - 5549 (2012)

A new method for C-C and C-N bond formation of heteroaromatics and C(sp3)-H alkanes was developed with high regioselectivity. The reaction occurred on C8 to give 8-cylcoakylpurines by C-C bond formation only promoted by tBuOOtBu, while it occurred on the amino group to give N6-alkylated purines by C-N bond formation when 2 equiv of CuI were added. A reaction mechanism was also proposed based on our preliminary experimental data.

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