Cas 870766-72-6,Methanesulfonic acid, trifluoro-, 7-methoxy-1-[4-[[(1R)-1-phenylethyl]amino]-1-phthalazinyl]-2-naphthalen yl ester

870766-72-6

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Basic information

Product Name: Methanesulfonic acid, trifluoro-, 7-methoxy-1-[4-[[(1R)-1-phenylethyl]amino]-1-phthalazinyl]-2-naphthalen yl ester
Synonyms:
CAS NO:870766-72-6
Molecular Formula: C28H22F3N3O4S
Molecular Weight: 553.562
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: Methanesulfonic acid, trifluoro-, 7-methoxy-1-[4-[[(1R)-1-phenylethyl]amino]-1-phthalazinyl]-2-naphthalen yl ester(CAS DataBase Reference)
NIST Chemistry Reference: Methanesulfonic acid, trifluoro-, 7-methoxy-1-[4-[[(1R)-1-phenylethyl]amino]-1-phthalazinyl]-2-naphthalen yl ester(870766-72-6)
EPA Substance Registry System: Methanesulfonic acid, trifluoro-, 7-methoxy-1-[4-[[(1R)-1-phenylethyl]amino]-1-phthalazinyl]-2-naphthalen yl ester(870766-72-6)

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: 870766-72-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 870766-72-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,0,7,6 and 6 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 870766-72:
(8*8)+(7*7)+(6*0)+(5*7)+(4*6)+(3*6)+(2*7)+(1*2)=206
206 % 10 = 6
So 870766-72-6 is a valid CAS Registry Number.

870766-72-6Upstream product

870766-72-6Downstream Products

870766-72-6Relevant academic research and scientific papers

Copper-catalyzed coupling of pyridines and quinolines with alkynes: A one-step, asymmetric route to functionalized heterocycles

Black, Daniel A.,Beveridge, Ramsay E.,Arndtsen, Bruce A.

, p. 1906 - 1910 (2008/09/18)

(Chemical Equation Presented) A copper (I)-catalyzed, asymmetric method to directly functionalize pyridines, quinolines, and isoquinolines with terminal alkynes is described. The reaction is readily diversified to incorporate a range of pyridine-based het

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