Cas 1146215-05-5,methyl 2,6-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-4-(trifluoromethyl)benzoate

1146215-05-5

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Basic information

Product Name: methyl 2,6-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-4-(trifluoromethyl)benzoate
Synonyms: methyl 2,6-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-4-(trifluoromethyl)benzoate
CAS NO:1146215-05-5
Molecular Formula:
Molecular Weight: 456.075
EINECS: N/A
Product Categories: N/A
Mol File: 1146215-05-5.mol
Article Data: 2

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: methyl 2,6-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-4-(trifluoromethyl)benzoate(CAS DataBase Reference)
NIST Chemistry Reference: methyl 2,6-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-4-(trifluoromethyl)benzoate(1146215-05-5)
EPA Substance Registry System: methyl 2,6-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-4-(trifluoromethyl)benzoate(1146215-05-5)

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: 1146215-05-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1146215-05-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,4,6,2,1 and 5 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1146215-05:
(9*1)+(8*1)+(7*4)+(6*6)+(5*2)+(4*1)+(3*5)+(2*0)+(1*5)=115
115 % 10 = 5
So 1146215-05-5 is a valid CAS Registry Number.

1146215-05-5Upstream product

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1146215-05-5Relevant articles and documents

Silyl phosphorus and nitrogen donor chelates for homogeneous ortho borylation catalysis

Ghaffari, Behnaz,Preshlock, Sean M.,Plattner, Donald L.,Staples, Richard J.,Maligres, Peter E.,Krska, Shane W.,Maleczka, Robert E.,Smith, Milton R.

, p. 14345 - 14348 (2014)

Ir catalysts supported by bidentate silyl ligands that contain P- or N-donors are shown to effect ortho borylations for a range of substituted aromatics. The substrate scope is broad, and the modular ligand synthesis allows for flexible catalyst design.

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