Cas 643745-03-3,2-{5-[6-chloro-5-(5-methyl-[1,2,4]oxadiazol-3-yl)-1H-indol-2-yl]-6-hydroxy-biphenyl-3-yl}-N,N-dimethyl-acetamide

643745-03-3

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Basic information

Product Name: 2-{5-[6-chloro-5-(5-methyl-[1,2,4]oxadiazol-3-yl)-1H-indol-2-yl]-6-hydroxy-biphenyl-3-yl}-N,N-dimethyl-acetamide
Synonyms: 2-{5-[6-chloro-5-(5-methyl-[1,2,4]oxadiazol-3-yl)-1H-indol-2-yl]-6-hydroxy-biphenyl-3-yl}-N,N-dimethyl-acetamide
CAS NO:643745-03-3
Molecular Formula:
Molecular Weight: 486.958
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-{5-[6-chloro-5-(5-methyl-[1,2,4]oxadiazol-3-yl)-1H-indol-2-yl]-6-hydroxy-biphenyl-3-yl}-N,N-dimethyl-acetamide(CAS DataBase Reference)
NIST Chemistry Reference: 2-{5-[6-chloro-5-(5-methyl-[1,2,4]oxadiazol-3-yl)-1H-indol-2-yl]-6-hydroxy-biphenyl-3-yl}-N,N-dimethyl-acetamide(643745-03-3)
EPA Substance Registry System: 2-{5-[6-chloro-5-(5-methyl-[1,2,4]oxadiazol-3-yl)-1H-indol-2-yl]-6-hydroxy-biphenyl-3-yl}-N,N-dimethyl-acetamide(643745-03-3)

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: 643745-03-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 643745-03-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,4,3,7,4 and 5 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 643745-03:
(8*6)+(7*4)+(6*3)+(5*7)+(4*4)+(3*5)+(2*0)+(1*3)=163
163 % 10 = 3
So 643745-03-3 is a valid CAS Registry Number.

643745-03-3Upstream product

643745-03-3Downstream Products

643745-03-3Relevant academic research and scientific papers

Environmentally friendly and efficient: Iron-mediated reduction of 3-methyl-5-aryl-1,2,4-oxadiazoles to benzamidines

Sendzik, Martin,Hui, Hon C.

, p. 8697 - 8700 (2007/10/03)

A new synthetic method is described for the mild and selective reduction of 3-methyl-5-aryl-1,2,4-oxadiazoles to amidines employing iron powder in aqueous medium. Its application is demonstrated in the synthesis of 1, a potent and selective urokinase-type plasminogen activator (uPA) inhibitor.

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