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153403-53-3

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153403-53-3 Usage

General Description

2-Chloro-6-fluorobenzo[d]oxazole is a chemical compound with the molecular formula C7H3ClFNO. It is a heterocyclic compound belonging to the oxazole class of organic compounds. This chemical is characterized by a chlorine atom attached to the second carbon atom of the benzene ring and a fluorine atom attached to the sixth carbon atom. It is used in the pharmaceutical industry for the synthesis of various biologically active compounds, including potential drugs. Its unique structure and properties make it a valuable building block for the development of new pharmaceuticals and agrochemicals. Additionally, research is ongoing to explore its potential applications in other fields, such as materials science and organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 153403-53-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,4,0 and 3 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 153403-53:
(8*1)+(7*5)+(6*3)+(5*4)+(4*0)+(3*3)+(2*5)+(1*3)=103
103 % 10 = 3
So 153403-53-3 is a valid CAS Registry Number.

153403-53-3Relevant articles and documents

NOVEL COMPOUNDS AND COMPOSITIONS FOR INHIBITION OF FASN

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Page/Page column 257, (2014/10/18)

The present invention relates to compounds and composition for inhibition of FASN, their synthesis, applications, and antidotes. An illustrative compound of the invention is shown below:

Analgesic Compounds, Compositions, and Uses Thereof

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Page/Page column 20, (2011/10/04)

The invention relates to compounds, compositions, and methods for diminishing pain in a subject in need thereof comprising administering the compounds and compositions herein described.

Synthesis and evaluation of arylaminoethyl amides as noncovalent inhibitors of cathepsin S. Part 3: Heterocyclic P3

Tully, David C.,Liu, Hong,Alper, Phil B.,Chatterjee, Arnab K.,Epple, Robert,Roberts, Michael J.,Williams, Jennifer A.,Nguyen, Khanhlinh T.,Woodmansee, David H.,Tumanut, Christine,Li, Jun,Spraggon, Glen,Chang, Jonathan,Tuntland, Tove,Harris, Jennifer L.,Karanewsky, Donald S.

, p. 1975 - 1980 (2007/10/03)

A series of Nα-2-benzoxazolyl-α-amino acid-(arylaminoethyl)amides were identified as potent, selective, and noncovalent inhibitors of cathepsin S. Structure-activity relationships including strategies for modulating the selectivities among cathepsins S, K, and L, and in vivo pharmacokinetics are discussed. A X-ray structure of compound 3 bound to the active site of cathepsin S is also reported.

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