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Diethyl [(5-chloro-1-benzothiophen-3-yl)Methyl]phosphonate is an organophosphorus compound characterized by the presence of a phosphonate group and a 5-chloro-1-benzothiophene ring. It is a versatile intermediate used in the synthesis of a range of pharmaceuticals, agrochemicals, and materials, and is valued for its potential in research and development within the realms of chemistry and medicinal chemistry.

862094-14-2

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862094-14-2 Usage

Uses

Used in Pharmaceutical Industry:
Diethyl [(5-chloro-1-benzothiophen-3-yl)Methyl]phosphonate is used as a chemical precursor for the synthesis of various pharmaceuticals. Its unique structure allows it to be a key component in the development of new drugs, particularly those targeting specific biological pathways or receptors.
Used in Agrochemical Industry:
In the agrochemical sector, Diethyl [(5-chloro-1-benzothiophen-3-yl)Methyl]phosphonate is utilized as a starting material for the creation of novel pesticides and herbicides. Its ability to be modified and incorporated into different chemical structures makes it a valuable asset in the design of effective and targeted agrochemicals.
Used in Materials Science:
Diethyl [(5-chloro-1-benzothiophen-3-yl)Methyl]phosphonate is also used as a building block in the development of new materials with specific properties. Its incorporation into polymers or other materials can lead to advancements in areas such as electronics, coatings, or specialty chemicals.
Used in Research and Development:
Diethyl [(5-chloro-1-benzothiophen-3-yl)Methyl]phosphonate is employed as a research tool in chemistry and medicinal chemistry labs. It aids scientists in exploring new reaction pathways, understanding molecular interactions, and developing innovative synthetic methods.
Safety Note:
It is crucial to handle and store Diethyl [(5-chloro-1-benzothiophen-3-yl)Methyl]phosphonate with care due to its potential hazards if not used properly, ensuring safety protocols are followed in research and industrial settings.

Check Digit Verification of cas no

The CAS Registry Mumber 862094-14-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,2,0,9 and 4 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 862094-14:
(8*8)+(7*6)+(6*2)+(5*0)+(4*9)+(3*4)+(2*1)+(1*4)=172
172 % 10 = 2
So 862094-14-2 is a valid CAS Registry Number.

862094-14-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name Diethyl [(5-chloro-1-benzothiophen-3-yl)methyl]phosphonate

1.2 Other means of identification

Product number -
Other names 5-chloro-3-(diethoxyphosphorylmethyl)-1-benzothiophene

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:862094-14-2 SDS

862094-14-2Relevant academic research and scientific papers

Discovery of potent, selective, orally active, nonpeptide inhibitors of human mast cell chymase

Greco, Michael N.,Hawkins, Michael J.,Powell, Eugene T.,Almond Jr., Harold R.,De Garavilla, Lawrence,Hall, Jeffrey,Minor, Lisa K.,Wang, Yuanping,Corcoran, Thomas W.,Di Cera, Enrico,Cantwell, Angelene M.,Savvides, Savvas N.,Damiano, Bruce P.,Maryanoff, Bruce E.

, p. 1727 - 1730 (2008/02/02)

A series of β-carboxamido-phosphon(in)ic acids (2) was identified as a new structural motif for obtaining potent inhibitors of human mast cell chymase. For example, 1-naphthyl derivative 5f had an IC50 value of 29 nM and (E)-styryl derivative 6

Novel inhibitors of chymase

-

Page/Page column 47, (2008/06/13)

The present invention is directed to a compound of formula (I), methods for preparing these compounds, compositions, intermediates and derivatives thereof, and methods for treating inflammatory and serine protease mediated disorders.

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