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1002334-12-4

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  • Featured products 1-Phenyl-4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole

    Cas No: 1002334-12-4

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1002334-12-4 Usage

General Description

1-Phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole is a chemical compound that contains a boron atom. It is commonly used in organic synthesis as a building block for the creation of various pharmaceuticals and agrochemicals. 1-Phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole has a pyrazole backbone with a phenyl group at one end and a boron-containing dioxaborolane group at the other end. The presence of the boron atom makes it a useful reagent for Suzuki-Miyaura cross-coupling reactions, which are important in the formation of carbon-carbon bonds in organic synthesis. Additionally, the tetramethyl substitution on the dioxaborolane moiety makes it particularly stable and less reactive toward protodeboronation, increasing its utility as a synthetic reagent. Overall, 1-Phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole is a valuable compound in organic synthesis due to its versatility and stability as a boron-containing reagent.

Check Digit Verification of cas no

The CAS Registry Mumber 1002334-12-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,2,3,3 and 4 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1002334-12:
(9*1)+(8*0)+(7*0)+(6*2)+(5*3)+(4*3)+(3*4)+(2*1)+(1*2)=64
64 % 10 = 4
So 1002334-12-4 is a valid CAS Registry Number.

1002334-12-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole

1.2 Other means of identification

Product number -
Other names 1-phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazole

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:1002334-12-4 SDS

1002334-12-4Relevant articles and documents

Potent and orally bioavailable CDK8 inhibitors: Design, synthesis, structure-activity relationship analysis and biological evaluation

Yu, Mingfeng,Teo, Theodosia,Yang, Yuchao,Li, Manjun,Long, Yi,Philip, Stephen,Noll, Benjamin,Heinemann, Gary K.,Diab, Sarah,Eldi, Preethi,Mekonnen, Laychiluh,Anshabo, Abel T.,Rahaman, Muhammed H.,Milne, Robert,Hayball, John D.,Wang, Shudong

, (2021)

CDK8 regulates transcription either by phosphorylation of transcription factors or, as part of a four-subunit kinase module, through a reversible association of the kinase module with the Mediator complex, a highly conserved transcriptional coactivator. D

HETEROARYL COMPOUNDS AND PHARMACEUTICAL APPLICATIONS THEREOF

-

Paragraph 00690, (2016/01/25)

The present invention provides herein is a heteroaryl compound or a stereoisomer, a geometric isomer, a tautomer, a racemate, an N-oxide, a hydrate, a solvate, a metabolite, a pharmaceutically acceptable salt or a prodrug thereof, as well as a pharmaceutical composition containing the compound disclosed herein. The present invention also provides herein is use of the compound or the pharmaceutical composition thereof disclosed herein in the manufacture of a medicine for treating autoimmune diseases or proliferative diseases.

Investigation of the scope and regiochemistry of alkynylboronate cycloadditions with sydnones

Browne, Duncan L.,Vivat, Jerome F.,Plant, Andrew,Gomez-Bengoa, Enrique,Harrity, Joseph P. A.

supporting information; experimental part, p. 7762 - 7769 (2009/10/16)

The cycloaddition of alkynylboronates and sydnones provides a convenientand highly regioselective method for the synthesis of a broad range of di-, tri-, and tetrasubstituted pyrazole boronic esters. The origins of an observed regiochemical divergence in the reactions of terminal alkyny lboronates with their more substituted analogues have been studied by DFT methods.

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