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4-(4-Bromo-3-(1,3-dioxolan-2-yl)phenoxy)benzonitrile is a chemical compound characterized by the molecular formula C15H11BrNO3. It is a white to off-white solid that is primarily utilized in pharmaceutical research as a building block for the synthesis of innovative compounds. 4-(4-BroMo-3-(1,3-dioxolan-2-yl)phenoxy)benzonitrile is known for its potential applications in the development of drugs across various therapeutic areas, including oncology and neurology, as well as for its potential antimicrobial and antifungal properties. Its unique structure and properties also make it a candidate for use in the development of agrochemicals and materials science. However, due to its potentially hazardous nature, it should be handled with care and only by trained professionals in a laboratory setting.

1217366-74-9

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1217366-74-9 Usage

Uses

Used in Pharmaceutical Research:
4-(4-Bromo-3-(1,3-dioxolan-2-yl)phenoxy)benzonitrile is used as a building block for the synthesis of novel compounds in pharmaceutical research, contributing to the development of new drugs for various therapeutic areas.
Used in Oncology:
In the field of oncology, 4-(4-Bromo-3-(1,3-dioxolan-2-yl)phenoxy)benzonitrile is used as a potential component in the development of anticancer drugs, targeting the synthesis of compounds that can combat cancer cells.
Used in Neurology:
4-(4-Bromo-3-(1,3-dioxolan-2-yl)phenoxy)benzonitrile is utilized in neurology for the synthesis of compounds that may have therapeutic effects on neurological disorders, potentially leading to new treatments for such conditions.
Used in Antimicrobial and Antifungal Applications:
4-(4-BroMo-3-(1,3-dioxolan-2-yl)phenoxy)benzonitrile is studied for its potential antimicrobial and antifungal properties, suggesting its use in the development of new agents to combat microbial infections and fungal diseases.
Used in Agrochemical Development:
Due to its unique structure and properties, 4-(4-Bromo-3-(1,3-dioxolan-2-yl)phenoxy)benzonitrile may be used in the development of agrochemicals, potentially contributing to the creation of new pesticides or other agricultural chemicals.
Used in Materials Science:
4-(4-BroMo-3-(1,3-dioxolan-2-yl)phenoxy)benzonitrile's unique properties also make it a candidate for use in materials science, where it could be employed in the development of new materials with specific characteristics for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1217366-74-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,7,3,6 and 6 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1217366-74:
(9*1)+(8*2)+(7*1)+(6*7)+(5*3)+(4*6)+(3*6)+(2*7)+(1*4)=149
149 % 10 = 9
So 1217366-74-9 is a valid CAS Registry Number.

1217366-74-9SDS

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 4-(4-Bromo-3-(1,3-dioxolan-2-yl)phenoxy)benzonitrile

1.2 Other means of identification

Product number -
Other names 4-(4-Bromo-3-(1,3-dioxolan-2-yl)phenoxy)benzonitrile

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:1217366-74-9 SDS

1217366-74-9Relevant academic research and scientific papers

Discovery and structure-activity study of a novel benzoxaborole anti-inflammatory agent (AN2728) for the potential topical treatment of psoriasis and atopic dermatitis

Akama, Tsutomu,Baker, Stephen J.,Zhang, Yong-Kang,Hernandez, Vincent,Zhou, Huchen,Sanders, Virginia,Freund, Yvonne,Kimura, Richard,Maples, Kirk R.,Plattner, Jacob J.

scheme or table, p. 2129 - 2132 (2009/12/07)

A series of phenoxy benzoxaboroles were synthesized and screened for their inhibitory activity against PDE4 and cytokine release. 5-(4-Cyanophenoxy)-2,3-dihydro-1-hydroxy-2,1-benzoxaborole (AN2728) showed potent activity both in vitro and in vivo. This compound is now in clinical development for the topical treatment of psoriasis and being pursued for the topical treatment of atopic dermatitis.

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