Cas 1024677-08-4,N-(((2S,3aS,4R,6R,6aS)-6-(60(3-ethylureido)-9H-purin-9-yl)-2-styryltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)methyl)-2-hydroxyacetamide

1024677-08-4

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Basic information

Product Name: N-(((2S,3aS,4R,6R,6aS)-6-(60(3-ethylureido)-9H-purin-9-yl)-2-styryltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)methyl)-2-hydroxyacetamide
Synonyms: N-(((2S,3aS,4R,6R,6aS)-6-(60(3-ethylureido)-9H-purin-9-yl)-2-styryltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)methyl)-2-hydroxyacetamide
CAS NO:1024677-08-4
Molecular Formula:
Molecular Weight: 509.522
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-(((2S,3aS,4R,6R,6aS)-6-(60(3-ethylureido)-9H-purin-9-yl)-2-styryltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)methyl)-2-hydroxyacetamide(CAS DataBase Reference)
NIST Chemistry Reference: N-(((2S,3aS,4R,6R,6aS)-6-(60(3-ethylureido)-9H-purin-9-yl)-2-styryltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)methyl)-2-hydroxyacetamide(1024677-08-4)
EPA Substance Registry System: N-(((2S,3aS,4R,6R,6aS)-6-(60(3-ethylureido)-9H-purin-9-yl)-2-styryltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)methyl)-2-hydroxyacetamide(1024677-08-4)

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: 1024677-08-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1024677-08-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,4,6,7 and 7 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1024677-08:
(9*1)+(8*0)+(7*2)+(6*4)+(5*6)+(4*7)+(3*7)+(2*0)+(1*8)=134
134 % 10 = 4
So 1024677-08-4 is a valid CAS Registry Number.

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1024677-08-4Relevant academic research and scientific papers

Adenosine analogues as inhibitors of P2Y12 receptor mediated platelet aggregation

Douglass, James G.,deCamp, J. Bryan,Fulcher, Emilee H.,Jones, William,Mahanty, Sanjoy,Morgan, Anna,Smirnov, Dima,Boyer, Jose L.,Watson, Paul S.

, p. 2167 - 2171 (2008/12/22)

Modified adenosine derivatives may lead to the development of P2Y12 antagonists that are potent, selective, and bind reversibly to the receptor. Analogues of 2′,3′-trans-styryl acetal-N6-ureido-adenosine monophosphate were prepared by modificat

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