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2-Acetylpyridine-4-boronic acid pinacol ester is a chemical compound with the molecular formula C14H17BO4. It is a boronic acid ester derivative of the aromatic compound 2-acetylpyridine, known for its ability to form covalent bonds with other molecules. This versatile reactivity and potential applications in drug discovery and material science make it a compound of interest to researchers in various fields of chemistry.

741709-58-0

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741709-58-0 Usage

Uses

Used in Organic Chemistry:
2-Acetylpyridine-4-boronic acid pinacol ester is used as a reagent for the synthesis of various pharmaceuticals, agrochemicals, and materials. Its ability to form covalent bonds with other molecules makes it a useful tool in chemical synthesis.
Used in Drug Discovery:
As a building block in the preparation of new molecules, 2-Acetylpyridine-4-boronic acid pinacol ester is used for developing potential therapeutic applications. Its versatile reactivity allows for the creation of novel compounds with potential benefits in the medical field.
Used in Material Science:
2-Acetylpyridine-4-boronic acid pinacol ester is also utilized in material science for the development of new materials with unique properties. Its role as a building block contributes to the advancement of material technologies.

Check Digit Verification of cas no

The CAS Registry Mumber 741709-58-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,1,7,0 and 9 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 741709-58:
(8*7)+(7*4)+(6*1)+(5*7)+(4*0)+(3*9)+(2*5)+(1*8)=170
170 % 10 = 0
So 741709-58-0 is a valid CAS Registry Number.
InChI:InChI=1/C13H18BNO3/c1-9(16)11-8-10(6-7-15-11)14-17-12(2,3)13(4,5)18-14/h6-8H,1-5H3

741709-58-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl]ethanone

1.2 Other means of identification

Product number -
Other names 2-ACETYLPYRIDINE-4-BORONIC ACID PINACOL ESTER

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:741709-58-0 SDS

741709-58-0Downstream Products

741709-58-0Relevant academic research and scientific papers

Understanding the Activation of Air-Stable Ir(COD)(Phen)Cl Precatalyst for C-H Borylation of Aromatics and Heteroaromatics

Slack, Eric D.,Colacot, Thomas J.

supporting information, p. 1561 - 1565 (2021/02/20)

A newly developed robust catalyst [Ir(COD)(Phen)Cl] (A) was used for the C-H borylation of three dozen aromatics and heteroaromatics with excellent yield and selectivity. Activation of the catalyst was identified by the use of catalytic amounts of water, alcohols, etc., when B2pin2 was used in noncoordinating solvents, while for THF catalytic use of HBpin was required. The results were on par with the in situ based expensive system [Ir(OMe)(COD)]2/dtbbpy or Me4Phen.

SREBP INHIBITORS COMPRISING A 6-MEMBERED CENTRAL RING

-

Paragraph 0572, (2019/08/12)

Provided herein are compounds comprising a three-ring core, such as compounds of Formula (X), Formula (X-A), Formula (X-Ai), Formula (X-B), Formula (X-Bi), Formula (Z), Formula (Z-A), Formula (Z-Ai), Formula (Z-B), Formula (Z-Bi), Formula (I), Formula (I-A), Formula (I-Ai), Formula (I-B), and Formula (I-Bi), and pharmaceutically acceptable salts, solvates, tautomers, isotopes, or isomers thereof. Also provided herein are methods of inhibiting a component of the sterol regulatory element binding protein (SREBP) pathway, such as an SREBP or SREBP cleavage activating protein (SCAP), using these compounds, or pharmaceutically acceptable salts, solvates, tautomers, isotopes, or isomers thereof. Further provided are methods of treating a disorder in a subject in need thereof, such as liver disease, non-alcoholic steatohepatitis, insulin resistance, or cancer.

OXEPINOPYRAZOLE DERIVATIVES AS INHIBITORS OF PI3-KINASE ACTIVITY

-

Page/Page column 159, (2018/11/22)

The invention is directed to compounds of formula (I), and salts thereof. The compounds are inhibitors of kinase activity, in particular PI3-kinase activity.

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