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107624-44-2

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107624-44-2 Usage

Description

(Biphenyl-2-yloxy)-acetonitrile, with the molecular formula C14H11NO, is a chemical compound derived from biphenyl, an aromatic hydrocarbon. It features a nitrile group (-C≡N) and an alkoxy group (-O-) attached to the biphenyl ring, endowing it with unique chemical properties and reactivity.

Uses

Used in Organic Synthesis:
(Biphenyl-2-yloxy)-acetonitrile is used as a building block in organic synthesis for the preparation of other organic compounds. Its chemical structure allows for versatile reactions and modifications, making it a valuable component in the creation of a variety of molecules.
Used in Pharmaceutical Development:
In the pharmaceutical industry, (Biphenyl-2-yloxy)-acetonitrile is used as a key intermediate in the development of new drugs. Its unique structure can be tailored to interact with specific biological targets, potentially leading to the discovery of novel therapeutic agents.
Used in Agrochemicals:
(Biphenyl-2-yloxy)-acetonitrile also finds application in the agrochemical sector, where it is utilized in the synthesis of compounds with pesticidal or herbicidal properties, contributing to the development of more effective and targeted agricultural chemicals.
Used in Materials Science:
(Biphenyl-2-yloxy)-acetonitrile's structure and properties make it suitable for use in materials science, where it can be incorporated into the design and synthesis of new materials with specific properties, such as improved conductivity, strength, or stability.
Used as an Intermediate in Fine Chemicals Production:
(Biphenyl-2-yloxy)-acetonitrile serves as an intermediate in the production of various fine chemicals, which are high-purity chemicals used in various industries, including pharmaceuticals, fragrances, and flavors.
Used as a Reagent in Organic Reactions:
Due to its reactivity, (Biphenyl-2-yloxy)-acetonitrile can be employed as a reagent in a range of organic reactions, facilitating the synthesis of complex organic molecules and contributing to the advancement of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 107624-44-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,6,2 and 4 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 107624-44:
(8*1)+(7*0)+(6*7)+(5*6)+(4*2)+(3*4)+(2*4)+(1*4)=112
112 % 10 = 2
So 107624-44-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H11NO/c15-10-11-16-14-9-5-4-8-13(14)12-6-2-1-3-7-12/h1-9H,11H2

107624-44-2SDS

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 (2-Biphenylyloxy)acetonitrile

1.2 Other means of identification

Product number -
Other names [1,1'-Biphenyl]-2,3,3',4,4',5'-hexol

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:107624-44-2 SDS

107624-44-2Downstream Products

107624-44-2Relevant articles and documents

Iodoacetonitrile and bromoacetonitrile as alkylating reagents for the nitrogen-phosphorus detector

Shin, Ho-Sang,Kim, Seungki,Myung, Seung-Woon,Park, Jong-Sei

, p. 1853 - 1859 (2007/10/02)

Iodoacetonitrile and bromoacetonitrile were used to enhance the sensitivity of chromatographically difficult compounds. Selective derivatization occurs with acidic hydroxyl, amino, and amide functional groups but does not occur for the alcoholic hydroxyl

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