175135-69-0 Usage
Uses
Used in Pharmaceutical Industry:
2-(4-METHOXYPHENOXY)-5-NITROBENZENE-1-CARBONYL CHLORIDE is used as a reagent for the synthesis of pharmaceutical compounds, facilitating the introduction of the 5-nitrobenzene-1-carbonyl group into organic molecules. This contributes to the development of new drugs with specific therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 2-(4-METHOXYPHENOXY)-5-NITROBENZENE-1-CARBONYL CHLORIDE serves as a key intermediate in the synthesis of agrochemicals, enhancing the functional groups of these compounds to improve their effectiveness in agricultural applications.
Used in Dye and Pigment Manufacturing:
2-(4-METHOXYPHENOXY)-5-NITROBENZENE-1-CARBONYL CHLORIDE is utilized as an intermediate in the production of dyes and pigments, contributing to the creation of a diverse range of colorants for various industries, including textiles, plastics, and printing inks.
Used in Specialty Chemicals Production:
2-(4-METHOXYPHENOXY)-5-NITROBENZENE-1-CARBONYL CHLORIDE also plays a role in the manufacturing of specialty chemicals, where its unique properties allow for the development of high-performance materials for specific applications in industries such as coatings, adhesives, and sealants.
Check Digit Verification of cas no
The CAS Registry Mumber 175135-69-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,5,1,3 and 5 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 175135-69:
(8*1)+(7*7)+(6*5)+(5*1)+(4*3)+(3*5)+(2*6)+(1*9)=140
140 % 10 = 0
So 175135-69-0 is a valid CAS Registry Number.
InChI:InChI=1/C14H10ClNO5/c1-20-10-3-5-11(6-4-10)21-13-7-2-9(16(18)19)8-12(13)14(15)17/h2-8H,1H3
175135-69-0Relevant academic research and scientific papers
SUBSTITUTED CYCLOHEXYL-1,4-DIAMINE DERIVATIVES WITH A CHAIN EXTENSION
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Page/Page column 25, (2008/06/13)
The invention relates to substituted cyclohexyl-1,4-diamine derivatives, to a method for their production, to medicaments containing said compounds and to the use of substituted cyclohexyl-1,4-diamine derivatives for producing medicaments.
2-(4-Methoxyphenoxy)-5-nitro-N-(4-sulfamoylphenyl)benzamide activates Kir6.2/SUR1 KATP channels
Nielsen, Flemming E.,Jacobsen, Palle,Worsaae, Anne,Arkhammar, Per O.G.,Wahl, Philip,Bondo Hansen, John
, p. 5727 - 5730 (2007/10/03)
2-(4-Methoxyphenoxy)-5-nitro-N-(4-sulfamoylphenyl)benzamide and close analogues inhibit glucose stimulated insulin release through activation of Kir6.2/SUR1 KATP channels of beta cells.
