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269410-27-7

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269410-27-7 Usage

Description

N-(2-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetamide is a chemical compound characterized by its molecular formula C16H20BNO3F. It is a fluorinated acetamide derivative that features a boron-containing phenyl ring. N-(2-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetamide is known for its unique structure and properties, which make it a valuable asset in various fields of chemistry and material science.

Uses

Used in Organic Synthesis:
N-(2-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetamide is utilized as a reagent in organic synthesis, particularly for the formation of carbon-carbon and carbon-heteroatom bonds. Its unique structure allows it to facilitate these bond formations, making it a valuable tool in the synthesis of complex organic molecules.
Used in Pharmaceutical Development:
N-(2-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetamide also finds application in the development of pharmaceuticals. Its unique properties and reactivity make it a promising candidate for the creation of new drugs with potential therapeutic benefits.
Used in Agrochemical Development:
N-(2-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetamide is also used in the development of agrochemicals. Its potential to form various chemical bonds can contribute to the creation of new agrochemicals that can improve crop protection and yield.
Used in Chemistry and Material Science Research:
Due to its unique structure and properties, this compound has potential applications in various fields of chemistry and material science. Researchers can leverage its reactivity and structural features to explore new reactions, materials, and applications that can advance scientific knowledge and lead to innovative products.

Check Digit Verification of cas no

The CAS Registry Mumber 269410-27-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,9,4,1 and 0 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 269410-27:
(8*2)+(7*6)+(6*9)+(5*4)+(4*1)+(3*0)+(2*2)+(1*7)=147
147 % 10 = 7
So 269410-27-7 is a valid CAS Registry Number.
InChI:InChI=1/C14H19BFNO3/c1-9(18)17-12-7-6-10(8-11(12)16)15-19-13(2,3)14(4,5)20-15/h6-8H,1-5H3,(H,17,18)

269410-27-7SDS

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-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]acetamide

1.2 Other means of identification

Product number -
Other names 4-Acetamido-3-fluorophenylboronic acid,pinacol ester

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:269410-27-7 SDS

269410-27-7Downstream Products

269410-27-7Relevant articles and documents

NOVEL COMPOUNDS AS MODULATORS OF PROTEIN KINASES

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Page/Page column 122; 123, (2012/11/14)

The present invention provides PI3K protein kinase modulators, methods of preparing them, pharmaceutical compositions containing them and methods of treatment, prevention and/or amelioration of kinase mediated diseases or disorders with them.

Hydroboronation process

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Page column 69, (2010/02/05)

The invention relates to processes for the synthesis of aryl or alkene borates which comprises reacting: (i) an olefinic compound having a halogen or halogen-like substituent in a vinylic substitution position, or (ii) an aromatic ring having a halogen or halogen-like substituent in a ring substitution position, with a disubstituted monohydroborane in the presence of a Group 8-11 metal catalyst. The invention also relates to the use of these borates in coupling reactions. The invention further relates to certain disubstituted monohydroboranes and aryl or alkene borates.

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