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1-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]pyrrolidine is a boronic acid derivative with the molecular formula C22H31BO2N. It features a pyrrolidine ring and a boron-containing moiety, making it a versatile intermediate for the synthesis of complex organic molecules. This chemical compound is widely used in organic synthesis, particularly for the development of pharmaceuticals and agrochemicals. Its unique structure and reactivity, along with the high level of substitution on the boron atom, confer unique properties that make it a valuable tool in medicinal chemistry, drug discovery, and the development of new materials and catalysts.

857283-63-7

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857283-63-7 Usage

Uses

Used in Pharmaceutical Industry:
1-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]pyrrolidine is used as a building block for the synthesis of various pharmaceuticals. Its unique structure and reactivity enable the development of complex organic molecules with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, 1-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]pyrrolidine serves as a key intermediate for the synthesis of agrochemicals. Its versatile nature allows for the creation of molecules with pesticidal or herbicidal properties, contributing to the development of effective crop protection solutions.
Used in Medicinal Chemistry:
1-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]pyrrolidine is utilized as a valuable tool in medicinal chemistry for the design and synthesis of novel drug candidates. Its unique properties and reactivity facilitate the exploration of new chemical space and the optimization of drug-like molecules.
Used in Drug Discovery:
This boronic acid derivative plays a crucial role in drug discovery, where it is employed to identify and develop new therapeutic agents. Its unique structural features and reactivity make it an attractive starting point for the synthesis of potential drug candidates.
Used in the Development of New Materials and Catalysts:
1-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]pyrrolidine is also used in the development of new materials and catalysts. Its boron-containing moiety and high level of substitution on the boron atom provide unique properties that can be harnessed for the creation of innovative materials and catalysts with diverse applications in chemical research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 857283-63-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,7,2,8 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 857283-63:
(8*8)+(7*5)+(6*7)+(5*2)+(4*8)+(3*3)+(2*6)+(1*3)=207
207 % 10 = 7
So 857283-63-7 is a valid CAS Registry Number.
InChI:InChI=1/C16H24BNO2/c1-15(2)16(3,4)20-17(19-15)13-8-7-9-14(12-13)18-10-5-6-11-18/h7-9,12H,5-6,10-11H2,1-4H3

857283-63-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[3-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PHENYL]PYRROLIDINE

1.2 Other means of identification

Product number -
Other names 1-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)pyrrolidine

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:857283-63-7 SDS

857283-63-7Relevant academic research and scientific papers

Remote steric control for undirected meta-selective C-H activation of arenes

Asako, Sobi,Ilies, Laurean,Jin, Yushu,Ramadoss, Boobalan

, p. 658 - 663 (2022/02/21)

Regioselective functionalization of arenes remains a challenging problem in organic synthesis. Steric interactions are often used to block sites adjacent to a given substituent, but they do not distinguish the remaining remote sites. We report a strategy

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