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254892-99-4

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254892-99-4 Usage

Description

3-(4-Boronophenyl)cyclobutanone ethylene ketal is a boron-containing cyclobutanone derivative with the molecular formula C12H14BO2. It features a unique structure that includes a boron atom and an ethylene ketal functional group, which together confer special reactivity and properties to the compound. This characteristic makes it a promising candidate for various applications in organic synthesis and materials science.

Uses

Used in Organic Synthesis:
3-(4-Boronophenyl)cyclobutanone ethylene ketal is used as a synthetic intermediate for the creation of new chemical compounds. Its boron atom and ethylene ketal group provide unique reactivity, facilitating various chemical transformations and synthetic pathways.
Used in Materials Science:
In the field of materials science, 3-(4-Boronophenyl)cyclobutanone ethylene ketal is utilized for the development of novel materials. 3-(4-BORONOPHENYL)CYCLOBUTANONE ETHYLENE KETAL's unique structure and reactivity can contribute to the design and synthesis of advanced materials with specific properties for various applications.
Used in Pharmaceutical Industry:
3-(4-Boronophenyl)cyclobutanone ethylene ketal is used as a building block in the pharmaceutical industry for the synthesis of potential drug candidates. Its unique chemical properties can be leveraged to create new molecules with therapeutic potential.
Used in Chemical Research:
In the realm of chemical research, 3-(4-Boronophenyl)cyclobutanone ethylene ketal serves as a subject of study to explore its reactivity and properties. Understanding its behavior in different chemical environments can lead to the discovery of new reactions and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 254892-99-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,4,8,9 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 254892-99:
(8*2)+(7*5)+(6*4)+(5*8)+(4*9)+(3*2)+(2*9)+(1*9)=184
184 % 10 = 4
So 254892-99-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H15BO4/c14-13(15)11-3-1-9(2-4-11)10-7-12(8-10)16-5-6-17-12/h1-4,10,14-15H,5-8H2

254892-99-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name [4-(5,8-dioxaspiro[3.4]octan-2-yl)phenyl]boronic acid

1.2 Other means of identification

Product number -
Other names OR7163

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:254892-99-4 SDS

254892-99-4Relevant articles and documents

4-Dihydroxyborylphenyl Analogues of 1-Aminocyclobutanecarboxylic Acids: Potential Boron Neutron Capture Therapy Agents

Srivastava, Rajiv R.,Singhaus, Robert R.,Kabalka, George W.

, p. 8495 - 8500 (2007/10/03)

A series of 4-dihydroxyborylphenyl analogues of an unnatural α-amino acid, 1-aminocyclobutanecarboxylic acid (ACBC), was synthesized. Varying numbers of methylene units were introduced between the 4-boronophenyl and ACBC moieties in order to introduce different degrees of lipophilicity into the molecules. The key step in the syntheses was the preparation of the precursor p-boronophenyl-substituted cyclobutanones which were subsequently converted to the desired amino acids via the Bucherer-Strecker reaction.

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