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Boronic acid, [2-[(diethylamino)carbonyl]-5-methoxyphenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

185033-59-4

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185033-59-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 185033-59-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,5,0,3 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 185033-59:
(8*1)+(7*8)+(6*5)+(5*0)+(4*3)+(3*3)+(2*5)+(1*9)=134
134 % 10 = 4
So 185033-59-4 is a valid CAS Registry Number.

185033-59-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-methoxy-2-(N,N-diethylcarboxamido)phenylboronic acid

1.2 Other means of identification

Product number -
Other names {2-[(diethylamino)carbonyl]-5-methoxyphenyl}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:185033-59-4 SDS

185033-59-4Relevant academic research and scientific papers

The directed ortho metalation - Palladium catalyzed cross coupling connection. A general regiospecific route to 9-phenanthrols and phenanthrenes. Exploratory further metalation

Fu, Jian-Min,Snieckus, Victor

, p. 905 - 919 (2007/10/03)

A new general and regiospecific synthesis of 9-phenanthrols (1 + 2 → 3 → 4, Scheme 1, Table 1) proceeding by a Directed ortho Metalation (DoM), Suzuki-Miyaura crocs coupling, and a new LDA-mediated Directed remote Metalation sequence is described. The facile Pd-catalyzed hydrogenolysis of the phenanthrols 4 into the corresponding phenanthrenes 5 via their triflates 18 translates the original DoM regioselectivity also into a general synthesis of phenanthrenes (Table 2). Further DoM (19 → 20, 21; 24 → 25), cross coupling (20c → 23), as well as oxidation - ring contraction (4b, 4f → 28a, 28b) chemistry of phenanthrene derivatives is reported.

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