Cas 1334181-20-2,1,3-di-tert-butyl-5-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene

1334181-20-2

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Basic information

Product Name: 1,3-di-tert-butyl-5-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene
Synonyms: 1,3-di-tert-butyl-5-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene
CAS NO:1334181-20-2
Molecular Formula:
Molecular Weight: 330.319
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: 1,3-di-tert-butyl-5-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene(CAS DataBase Reference)
NIST Chemistry Reference: 1,3-di-tert-butyl-5-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene(1334181-20-2)
EPA Substance Registry System: 1,3-di-tert-butyl-5-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene(1334181-20-2)

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: 1334181-20-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1334181-20-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,4,1,8 and 1 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1334181-20:
(9*1)+(8*3)+(7*3)+(6*4)+(5*1)+(4*8)+(3*1)+(2*2)+(1*0)=122
122 % 10 = 2
So 1334181-20-2 is a valid CAS Registry Number.

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1334181-20-2Relevant academic research and scientific papers

Palladium-catalyzed borylation of sterically demanding aryl halides with a silica-supported compact phosphane ligand

Kawamorita, Soichiro,Ohmiya, Hirohisa,Iwai, Tomohiro,Sawamura, Masaya

, p. 8363 - 8366 (2011)

Immobile but active: A silica-supported "compact" phosphane, Silica-SMAP, can be used in the Pd-catalyzed borylation of aryl chlorides or bromides with bis(pinacolato)diboron (see scheme). The Silica-SMAP/Pd system significantly expands the substrate scope of the borylation toward sterically and electronically challenging aryl halides.

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