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5-(TERT-BUTOXYCARBONYL)PYRIDINE-3-BORONIC ACID PINACOL ESTER is a boronic acid ester derivative featuring a pyridine ring and a tert-butoxycarbonyl (Boc) group. It is a significant compound in organic synthesis and medicinal chemistry, known for its role as a building block in the creation of pharmaceuticals, agrochemicals, and materials.
Used in Pharmaceutical Industry:
5-(TERT-BUTOXYCARBONYL)PYRIDINE-3-BORONIC ACID PINACOL ESTER is used as a key intermediate in the synthesis of complex organic molecules for drug development. Its Boc-protected pyridine moiety offers a versatile handle for further derivatization, facilitating the preparation of a wide range of pharmaceutical compounds.
Used in Agrochemical Industry:
In the agrochemical sector, 5-(TERT-BUTOXYCARBONYL)PYRIDINE-3-BORONIC ACID PINACOL ESTER is utilized as a building block for the synthesis of agrochemicals. Its ability to form stable complexes with reactive substrates makes it a valuable component in the development of effective and targeted agrochemical products.
Used in Materials Science:
5-(TERT-BUTOXYCARBONYL)PYRIDINE-3-BORONIC ACID PINACOL ESTER is employed as a component in the synthesis of advanced materials. Its involvement in carbon-carbon bond forming reactions, such as Suzuki-Miyaura cross-coupling, contributes to the creation of novel materials with specific properties for various applications.
Used in Organic Synthesis:
As a boronic acid ester derivative, 5-(TERT-BUTOXYCARBONYL)PYRIDINE-3-BORONIC ACID PINACOL ESTER is used in organic synthesis for its ability to form stable complexes with reactive substrates. This makes it a valuable tool in various carbon-carbon bond forming reactions, contributing to the synthesis of a broad spectrum of organic compounds.

1309982-38-4

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1309982-38-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1309982-38-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,0,9,9,8 and 2 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1309982-38:
(9*1)+(8*3)+(7*0)+(6*9)+(5*9)+(4*8)+(3*2)+(2*3)+(1*8)=184
184 % 10 = 4
So 1309982-38-4 is a valid CAS Registry Number.

1309982-38-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine-3-carboxylate

1.2 Other means of identification

Product number -
Other names -

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

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More Details:1309982-38-4 SDS

1309982-38-4Relevant academic research and scientific papers

NOVEL SPIROCHROMANONE CARBOXYLIC ACIDS

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Page/Page column 82-83, (2010/04/03)

The invention relates to a compound of a general formula (I): wherein A represents a linking group; Ar1 represents a group formed from an aromatic ring; R1 and R2 each independently represent a hydrogen atom, a halogen atom, a cyano group, a C2-C6 alkenyl group, a C1-C6 alkoxy group, a halo-C1-C6 alkoxy group, a cyclo-C3-C6 alkyloxy group, a C2-C7 alkanoyl group, a halo-C2-C7 alkanoyl group, a C2-C7 alkoxycarbonyl group, a halo-C2-C7 alkoxycarbonyl group, a cyclo-C3-C6 alkyloxycarbonyl group, an aralkyloxycarbonyl group, a carbamoyl-C1-C6 alkoxy group, a carboxy-C2-C6 alkenyl group, or a group of -Q1-N(Ra)-Q2-Rb; a C1-C6 alkyl group optionally having substituent(s); an aryl or heterocyclic group optionally having substituent(s); or a C1-C6 alkyl group or a C2-C6 alkenyl group having the aryl or heterocyclic group; T and U each independently represent a nitrogen atom or a methine group; and V represents an oxygen atom, a sulfur atom or an imino group. The compound of the invention is useful as therapeutical agents for various ACC-related diseases.

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