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Boronic acid, B-1H-pyrrolo[2,3-c]pyridin-4-yl-, is a boronic acid derivative characterized by the presence of a boronic acid functional group attached to a pyrrolopyridine ring structure. This unique structure endows it with the ability to bind to diols and other Lewis bases, making it a versatile compound in organic synthesis and medicinal chemistry. The B-1H-pyrrolo[2,3-c]pyridin-4-ylmoiety suggests its potential as a building block for the synthesis of pharmaceuticals or other biologically active compounds. Its specific chemical properties and potential applications depend on its structural and stereochemical features, as well as the reactions it can undergo in various chemical and biological environments.

1312368-90-3

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1312368-90-3 Usage

Uses

Used in Organic Synthesis:
Boronic acid, B-1H-pyrrolo[2,3-c]pyridin-4-yl-, is used as a reagent in organic synthesis for its ability to bind to diols and other Lewis bases. This property allows it to facilitate various chemical reactions, such as the formation of carbon-carbon bonds, making it a valuable tool in the synthesis of complex organic molecules.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, Boronic acid, B-1H-pyrrolo[2,3-c]pyridin-4-yl-, is used as a building block for the synthesis of pharmaceuticals and other biologically active compounds. Its unique structure and binding capabilities make it a promising candidate for the development of new drugs with novel mechanisms of action.
Used in Drug Design:
Boronic acid, B-1H-pyrrolo[2,3-c]pyridin-4-yl-, is used as a structural component in drug design for its potential to interact with biological targets, such as enzymes or receptors. Its ability to bind to diols and other Lewis bases can be exploited to create molecules with high affinity and selectivity for specific biological targets, leading to the development of more effective and targeted therapeutic agents.
Used in Chemical Biology:
In chemical biology, Boronic acid, B-1H-pyrrolo[2,3-c]pyridin-4-yl-, is used as a tool to study the interactions between small molecules and biological systems. Its ability to bind to diols and other Lewis bases can be utilized to probe the structure and function of proteins, nucleic acids, and other biomolecules, providing valuable insights into their mechanisms of action and potential therapeutic applications.
Used in Materials Science:
Boronic acid, B-1H-pyrrolo[2,3-c]pyridin-4-yl-, can be used in materials science for the development of new materials with unique properties. Its ability to bind to diols and other Lewis bases can be exploited to create self-assembling structures, functional coatings, or responsive materials that can interact with their environment in a controlled manner.

Check Digit Verification of cas no

The CAS Registry Mumber 1312368-90-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,2,3,6 and 8 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1312368-90:
(9*1)+(8*3)+(7*1)+(6*2)+(5*3)+(4*6)+(3*8)+(2*9)+(1*0)=133
133 % 10 = 3
So 1312368-90-3 is a valid CAS Registry Number.

1312368-90-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1H-Pyrrolo[2,3-c]pyridin-4-ylboronic acid

1.2 Other means of identification

Product number -
Other names D-1672

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:1312368-90-3 SDS

1312368-90-3Downstream Products

1312368-90-3Relevant academic research and scientific papers

NAPHTHYRIDINES AS INHIBITORS OF HPK1

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Paragraph 0771; 0772, (2018/10/21)

Naphthyridine compounds and their use as inhibitors of HPK1 are described. The compounds are useful in treating HPK1-dependent disorders and enhancing an immune response. Also described are methods of inhibiting HPK1, methods of treating HPK1-dependent disorders, methods for enhancing an immune response, and methods for preparing the naphthyridine compounds.

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