Cas 1512864-16-2,2,2'-(3-(4-bromophenyl)propane-1,1-diyl)bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolane)

1512864-16-2

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Basic information

Product Name: 2,2'-(3-(4-bromophenyl)propane-1,1-diyl)bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolane)
Synonyms: 2,2'-(3-(4-bromophenyl)propane-1,1-diyl)bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolane)
CAS NO:1512864-16-2
Molecular Formula:
Molecular Weight: 451.017
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: 2,2'-(3-(4-bromophenyl)propane-1,1-diyl)bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolane)(CAS DataBase Reference)
NIST Chemistry Reference: 2,2'-(3-(4-bromophenyl)propane-1,1-diyl)bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolane)(1512864-16-2)
EPA Substance Registry System: 2,2'-(3-(4-bromophenyl)propane-1,1-diyl)bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolane)(1512864-16-2)

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: 1512864-16-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1512864-16-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,1,2,8,6 and 4 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1512864-16:
(9*1)+(8*5)+(7*1)+(6*2)+(5*8)+(4*6)+(3*4)+(2*1)+(1*6)=152
152 % 10 = 2
So 1512864-16-2 is a valid CAS Registry Number.

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1512864-16-2Relevant academic research and scientific papers

Formal carbon insertion of n-tosylhydrazone into B-B and B-Si bonds: Gem-diborylation and gem-silylborylation of sp3 carbon

Li, Huan,Shangguan, Xianghang,Zhang, Zhikun,Huang, Shan,Zhang, Yan,Wang, Jianbo

supporting information, p. 448 - 451 (2014/04/03)

A convenient method is developed to synthesize 1,1-diboronates from the corresponding N-tosylhydrazones. This method is also applicable to synthesize 1-silyl-1-boron compounds. Meanwhile, derivatization and consecutive Pd-catalyzed cross-coupling reaction

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