Cas 1417417-98-1,(4-(benzyloxy)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)(phenyl)iodonium tosylate

1417417-98-1

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Basic information

Product Name: (4-(benzyloxy)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)(phenyl)iodonium tosylate
Synonyms:
CAS NO:1417417-98-1
Molecular Formula:
Molecular Weight: 684.4
EINECS: N/A
Product Categories: N/A
Mol File: 1417417-98-1.mol
Article Data: 1

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: (4-(benzyloxy)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)(phenyl)iodonium tosylate(CAS DataBase Reference)
NIST Chemistry Reference: (4-(benzyloxy)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)(phenyl)iodonium tosylate(1417417-98-1)
EPA Substance Registry System: (4-(benzyloxy)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)(phenyl)iodonium tosylate(1417417-98-1)

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: 1417417-98-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1417417-98-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,7,4,1 and 7 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1417417-98:
(9*1)+(8*4)+(7*1)+(6*7)+(5*4)+(4*1)+(3*7)+(2*9)+(1*8)=161
161 % 10 = 1
So 1417417-98-1 is a valid CAS Registry Number.

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1417417-98-1Relevant articles and documents

Synthesis of boron-substituted diaryliodonium salts and selective transformation into functionalized aryl boronates

Ito, Motoki,Itani, Itsuki,Toyoda, Yosuke,Morimoto, Koji,Dohi, Toshifumi,Kita, Yasuyuki

supporting information, p. 12555 - 12558 (2013/02/22)

Dormant boron awaits its true destiny in diaryliodonium salts synthesized from aryl boronate derivatives according to two alternative general methods with hypervalent iodine(III) reagents and fluoroalcohol solvents: transformation of an aryl C-H bond and

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