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454185-98-9

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  • Benzeneacetic acid, 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-,methyl ester Manufacturer/High quality/Best price/In stock

    Cas No: 454185-98-9

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  • Factory Price OLED 99% 454185-98-9 (4-METHOXYCARBONYLMETHYLPHENYL)BORONIC ACID PINACOL ESTER Manufacturer

    Cas No: 454185-98-9

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454185-98-9 Usage

Uses

(4-Methoxycarbonylmethyl)phenylboronic acid pinacol ester

Check Digit Verification of cas no

The CAS Registry Mumber 454185-98-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,5,4,1,8 and 5 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 454185-98:
(8*4)+(7*5)+(6*4)+(5*1)+(4*8)+(3*5)+(2*9)+(1*8)=169
169 % 10 = 9
So 454185-98-9 is a valid CAS Registry Number.
InChI:InChI=1/C15H21BO4/c1-14(2)15(3,4)20-16(19-14)12-8-6-11(7-9-12)10-13(17)18-5/h6-9H,10H2,1-5H3

454185-98-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetate

1.2 Other means of identification

Product number -
Other names methyl 2-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]acetate

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:454185-98-9 SDS

454185-98-9Relevant articles and documents

HETEROCYCLIC GLP-1 AGONISTS

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Page/Page column 118-120, (2021/11/06)

This disclosure relates to GLP-1 agonists of Formula (I): including pharmaceutically acceptable salts and solvates thereof, and pharmaceutical compositions including the same.

Pd-Catalyzed Site-Selective Borylation of Simple Arenes via Thianthrenation?

Chen, Xiao-Yue,Huang, Yu-Hao,Zhou, Jian,Wang, Peng

, p. 1269 - 1272 (2020/08/13)

Site-selective borylation of simple arenes was realized in one pot via an electrophilic thianthrenation/Pd-catalyzed borylation sequence. The key to achieve this operatically simple process is the use of Pd catalysis, which could tolerate the solvent and acidic conditions used in the thianthrenation step. This protocol features mild conditions, broad functional group tolerance, and simple manipulations, and is suitable for late-stage functionalization of a wide range of pharmaceuticals and complex bioactive molecules.

MOLECULES HAVING CERTAIN PESTICIDAL UTILITIES, INTERMEDIATES, COMPOSITIONS, AND PROCESSES, RELATED THERETO

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, (2016/02/18)

This disclosure relates to the field of molecules having pesticidal utility against pests in Phyla Nematoda, Arthropoda, and/or Mollusca, processes to produce such molecules and intermediates used in such processes, compositions containing such molecules, and processes of using such molecules against such pests. These molecules may be used, for example, as nematicides, acaricides, insecticides, miticides, and/or molluscicides. This document discloses molecules having the following formula (“Formula One”).

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