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6-(pyridin-3-yloxy)pyridine-3-boronic acid is a boronic acid derivative featuring a pyridine ring substituted by a pyridin-3-yloxy group. This chemical compound is a valuable building block in organic synthesis and medicinal chemistry, known for its ability to form stable complexes with diols and participate in carbon-carbon bond formation through cross-coupling reactions. Its unique structure and properties make it an important chemical in the fields of chemical synthesis and drug discovery.

918138-38-2

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918138-38-2 Usage

Uses

Used in Organic Synthesis:
6-(pyridin-3-yloxy)pyridine-3-boronic acid is used as a versatile building block for the synthesis of biologically active compounds and pharmaceuticals. Its ability to form stable complexes with diols and participate in cross-coupling reactions makes it a valuable tool in organic chemistry.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 6-(pyridin-3-yloxy)pyridine-3-boronic acid is utilized as a key intermediate for the development of new drugs. Its unique structure allows for the creation of novel compounds with potential therapeutic applications.
Used in Drug Discovery:
6-(pyridin-3-yloxy)pyridine-3-boronic acid is employed as a starting material in drug discovery processes. Its reactivity and compatibility with various chemical reactions enable the synthesis of diverse drug candidates with potential therapeutic benefits.
Used in Chemical Research:
6-(pyridin-3-yloxy)pyridine-3-boronic acid is also used in chemical research to explore new reaction pathways and develop innovative synthetic methods. Its unique properties make it an interesting subject for study in the realm of chemical science.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 6-(pyridin-3-yloxy)pyridine-3-boronic acid is used as a key component in the synthesis of new drug molecules. Its versatility and reactivity contribute to the development of innovative medications with improved efficacy and safety profiles.

Check Digit Verification of cas no

The CAS Registry Mumber 918138-38-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,8,1,3 and 8 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 918138-38:
(8*9)+(7*1)+(6*8)+(5*1)+(4*3)+(3*8)+(2*3)+(1*8)=182
182 % 10 = 2
So 918138-38-2 is a valid CAS Registry Number.

918138-38-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (6-pyridin-3-yloxypyridin-3-yl)boronic acid

1.2 Other means of identification

Product number -
Other names 6-(PYRIDIN-3-YLOXY)PYRIDINE-3-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:918138-38-2 SDS

918138-38-2Downstream Products

918138-38-2Relevant academic research and scientific papers

Novel oxybispyridylboronic acids: synthesis and study of their reactivity in Suzuki-type cross-coupling reactions

Voisin, Anne Sophie,Bouillon, Alexandre,Berenguer, Inmaculada,Lancelot, Jean-Charles,Lesnard, Aurélien,Rault, Sylvain

, p. 11734 - 11739 (2007/10/03)

This paper sets forth the synthesis of novel oxybispyridylboronic acids, which are prepared from the corresponding halo-oxybispyridines via halogen-metal exchange using n-butyllithium and treatment with triisopropylborate. A range of efficient cross-coupl

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