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N-(2-Fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)-2-methylpropan-2-amine is a complex organic chemical compound characterized by its molecular formula C18H28BFNO. It is a benzylamine derivative that incorporates a fluorine atom, a boron atom, and a methyl group within its structure. N-(2-Fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)-2-methylpropan-2-amine is recognized for its role in organic synthesis and medicinal chemistry, where it serves as a crucial building block for the creation of a variety of pharmaceuticals and biologically active molecules.

1256360-52-7

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1256360-52-7 Usage

Uses

Used in Organic Synthesis:
N-(2-Fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)-2-methylpropan-2-amine is utilized as a key intermediate in organic synthesis for the preparation of complex organic molecules. Its unique structural features, including the presence of fluorine and boron atoms, facilitate specific types of chemical reactions that are essential in the synthesis of target compounds.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, N-(2-Fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)-2-methylpropan-2-amine is employed as a building block for the development of new pharmaceuticals. Its incorporation into drug candidates can potentially enhance their pharmacological properties, such as potency, selectivity, and bioavailability, making it a valuable component in the design and synthesis of novel therapeutic agents.
Used in Drug Discovery Research:
N-(2-Fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)-2-methylpropan-2-amine also serves as a valuable tool in drug discovery research. Its unique structural elements allow researchers to investigate the effects of specific chemical groups on the biological activity of molecules, providing insights that can guide the optimization of drug candidates.
Used in the Development of Biologically Active Molecules:
N-(2-Fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)-2-methylpropan-2-amine is also used in the development of biologically active molecules, which can have potential applications in various therapeutic areas. Its versatility in chemical modifications makes it an important component in the creation of molecules with specific biological targets and mechanisms of action.
Overall, N-(2-Fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)-2-methylpropan-2-amine is a significant compound in the realms of chemistry and drug discovery, with its applications spanning across multiple industries and research areas.

Check Digit Verification of cas no

The CAS Registry Mumber 1256360-52-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,6,3,6 and 0 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1256360-52:
(9*1)+(8*2)+(7*5)+(6*6)+(5*3)+(4*6)+(3*0)+(2*5)+(1*2)=147
147 % 10 = 7
So 1256360-52-7 is a valid CAS Registry Number.

1256360-52-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[[2-fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methyl]-2-methylpropan-2-amine

1.2 Other means of identification

Product number -
Other names X0486

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 -
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More Details:1256360-52-7 SDS

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