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4-ISOTHIOCYANATOPHENYL ETHER, also known as 4-phenylisothiocyanate, is an aromatic isothiocyanate derivative with the molecular formula C7H5NOS. It is a chemical compound known for its strong odor and is widely used in organic synthesis and medicinal chemistry. The unique chemical properties of 4-ISOTHIOCYANATOPHENYL ETHER make it a versatile reagent for the preparation of pharmaceuticals, agrochemicals, and the modification of biomolecules. It also plays a significant role in the study of various biological processes and has potential applications in the development of new materials for industrial and academic purposes.

10396-05-1

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10396-05-1 Usage

Uses

Used in Pharmaceutical Industry:
4-ISOTHIOCYANATOPHENYL ETHER is used as a reagent for the synthesis of various pharmaceuticals due to its ability to form active compounds with therapeutic properties. Its strong reactivity with biomolecules allows for the development of new drugs with improved efficacy and selectivity.
Used in Agrochemical Industry:
In the agrochemical industry, 4-ISOTHIOCYANATOPHENYL ETHER is used as a precursor for the synthesis of various agrochemicals, including pesticides and herbicides. Its unique chemical properties enable the creation of effective and targeted agrochemicals for crop protection and management.
Used in Organic Synthesis:
4-ISOTHIOCYANATOPHENYL ETHER is used as a key intermediate in organic synthesis for the preparation of a wide range of organic compounds. Its strong reactivity with various functional groups makes it a valuable building block for the synthesis of complex organic molecules.
Used in Medicinal Chemistry:
In medicinal chemistry, 4-ISOTHIOCYANATOPHENYL ETHER is employed as a reagent for the modification of biomolecules, such as proteins and peptides. Its ability to form stable thiourea linkages allows for the development of novel bioconjugates with potential applications in drug delivery and targeted therapies.
Used in Material Science:
4-ISOTHIOCYANATOPHENYL ETHER has potential applications in the development of new materials for industrial and academic purposes. Its unique chemical properties can be utilized to create novel materials with specific properties, such as improved thermal stability, chemical resistance, or biocompatibility.
Used in Biological Research:
In biological research, 4-ISOTHIOCYANATOPHENYL ETHER is used as a tool for the study of various biological processes. Its ability to modify biomolecules and form stable linkages allows researchers to investigate the structure, function, and interactions of proteins and other biological molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 10396-05-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,9 and 6 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 10396-05:
(7*1)+(6*0)+(5*3)+(4*9)+(3*6)+(2*0)+(1*5)=81
81 % 10 = 1
So 10396-05-1 is a valid CAS Registry Number.
InChI:InChI=1/C14H8N2OS2/c18-9-15-11-1-5-13(6-2-11)17-14-7-3-12(4-8-14)16-10-19/h1-8H

10396-05-1SDS

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 4-Isothiocyanatophenyl ether

1.2 Other means of identification

Product number -
Other names 1-isothiocyanato-4-(4-isothiocyanatophenoxy)benzene

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:10396-05-1 SDS

10396-05-1Upstream product

10396-05-1Downstream Products

10396-05-1Relevant articles and documents

A FACILE NEW METHOD FOR THE PREPARATION OF AROMATIC DIISOTHIOCYANATES

Garin, J.,Melendez, E.,Merchan, F.,Merino, P.,Tejero, T.

, p. 289 - 290 (2007/10/02)

In the present communication we describe a new facile method for the preparation of aromatic diisothiocyanates.The main advantage of this method is a one-pot procedure from bis(dithiocarbamates) compared with the methods described in the literature.

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