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148345-64-6

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148345-64-6 Usage

Uses

Reactant for:? ;Pd-catalyzed Suzuki-Miyaura reaction1,2,3

Check Digit Verification of cas no

The CAS Registry Mumber 148345-64-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,8,3,4 and 5 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 148345-64:
(8*1)+(7*4)+(6*8)+(5*3)+(4*4)+(3*5)+(2*6)+(1*4)=146
146 % 10 = 6
So 148345-64-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H13BO3/c1-2-16-11-8-7-9-5-3-4-6-10(9)12(11)13(14)15/h3-8,14-15H,2H2,1H3

148345-64-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Ethoxy-1-naphthaleneboronic acid

1.2 Other means of identification

Product number -
Other names (2-ethoxynaphthalen-1-yl)boronic acid

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:148345-64-6 SDS

148345-64-6Relevant articles and documents

Palladium-Catalyzed Enantioselective Synthesis of 2-Aryl Cyclohex-2-enone Atropisomers: Platform Molecules for the Divergent Synthesis of Axially Chiral Biaryl Compounds

Pan, Chongqing,Zhu, Zixi,Zhang, Mingkai,Gu, Zhenhua

, p. 4777 - 4781 (2017)

The palladium-catalyzed asymmetric synthesis of enone-based atropisomers from 2-iodo-3-methylcyclohex-2-enones and aryl boronic acid is reported. BoPhoz-type phosphine–aminophosphine ligands showed superior enantioselectivity over other ligands. These cyc

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