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1048647-68-2

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1048647-68-2 Usage

Uses

3-(N-Benzylaminocarbonyl)phenylboronic acid, pinacol ester

Check Digit Verification of cas no

The CAS Registry Mumber 1048647-68-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,8,6,4 and 7 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1048647-68:
(9*1)+(8*0)+(7*4)+(6*8)+(5*6)+(4*4)+(3*7)+(2*6)+(1*8)=172
172 % 10 = 2
So 1048647-68-2 is a valid CAS Registry Number.

1048647-68-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name N-benzyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide

1.2 Other means of identification

Product number -
Other names N-benzyl-3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-benzamide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1048647-68-2 SDS

1048647-68-2Relevant articles and documents

Hydrogen Bond Directed ortho-Selective C?H Borylation of Secondary Aromatic Amides

Bai, Shao-Tao,Bheeter, Charles B.,Reek, Joost N. H.

supporting information, p. 13039 - 13043 (2019/07/31)

Reported is an iridium catalyst for ortho-selective C?H borylation of challenging secondary aromatic amide substrates, and the regioselectivity is controlled by hydrogen-bond interactions. The BAIPy-Ir catalyst forms three hydrogen bonds with the substrate during the crucial activation step, and allows ortho-C?H borylation with high selectivity. The catalyst displays unprecedented ortho selectivities for a wide variety of substrates that differ in electronic and steric properties, and the catalyst tolerates various functional groups. The regioselective C?H borylation catalyst is readily accessible and converts substrates on gram scale with high selectivity and conversion.

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