Cas 1451870-33-9,N,N,N',N'-tetramethyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)terephthalamide

1451870-33-9

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Basic information

Product Name: N,N,N',N'-tetramethyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)terephthalamide
Synonyms:
CAS NO:1451870-33-9
Molecular Formula:
Molecular Weight: 346.234
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,N,N',N'-tetramethyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)terephthalamide(CAS DataBase Reference)
NIST Chemistry Reference: N,N,N',N'-tetramethyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)terephthalamide(1451870-33-9)
EPA Substance Registry System: N,N,N',N'-tetramethyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)terephthalamide(1451870-33-9)

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: 1451870-33-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1451870-33-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,1,8,7 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1451870-33:
(9*1)+(8*4)+(7*5)+(6*1)+(5*8)+(4*7)+(3*0)+(2*3)+(1*3)=159
159 % 10 = 9
So 1451870-33-9 is a valid CAS Registry Number.

1451870-33-9Upstream product

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1451870-33-9Relevant academic research and scientific papers

Structure, theoretical studies, and coupling reactions of some new cyclic boronic esters

Kuttler, Andrew,Durganala, Sravanthi,Fratini, Albert,Morgan, Alexander B.,Benin, Vladimir

, p. 361 - 371 (2013/09/23)

The present report describes the X-ray structural and theoretical studies of some new pinacolboronate esters, and it also outlines the use of the target structures in Suzuki coupling reactions to produce new aromatic or heteroaromatic esters and amides. X

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