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N-(4-hydroxyphenyl)-1-naphthamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 223272-49-9 Structure
  • Basic information

    1. Product Name: N-(4-hydroxyphenyl)-1-naphthamide
    2. Synonyms: N-(4-hydroxyphenyl)-1-naphthamide
    3. CAS NO:223272-49-9
    4. Molecular Formula: C17H13NO2
    5. Molecular Weight: 263.29062
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 223272-49-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: N-(4-hydroxyphenyl)-1-naphthamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(4-hydroxyphenyl)-1-naphthamide(223272-49-9)
    11. EPA Substance Registry System: N-(4-hydroxyphenyl)-1-naphthamide(223272-49-9)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 223272-49-9(Hazardous Substances Data)

223272-49-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 223272-49-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,3,2,7 and 2 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 223272-49:
(8*2)+(7*2)+(6*3)+(5*2)+(4*7)+(3*2)+(2*4)+(1*9)=109
109 % 10 = 9
So 223272-49-9 is a valid CAS Registry Number.

223272-49-9Relevant articles and documents

INHIBITORS OF DIHYDROCERAMIDE DESATURASE FOR TREATING DISEASE

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Paragraph 00247; 00259, (2018/09/11)

Disclosed herein are dihydroceramide desaturase 1 (Des1) inhibitor compounds and compositions, which are useful in the treatment of diseases, such as metabolic, cardiovascular, fibrotic, autoimmune/chronic inflammatory diseases, cystic fibrosis, various cancers, neurodegenerative diseases, lipid storage disorders, and ischemia/reperfusion injury, where inhibition of Des1 is expected to be therapeutic to a patient. Methods of inhibition of Des1 activity in a human or animal subject are also provided.

Composition containing fluorescence-generating substrate

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, (2008/06/13)

A fluorescent dye-forming composition is provided that contains a fluorescence-generating substrate of formula (I): where R1 and R2 are each independently a hydrogen atom, or an electron-donating group selected from a lower alkyl gro

Anionic Micellar Effects on the Benzophenone-sensitized Photolysis of N-(1-Naphthoyl)-N-phenyl-O-benzoylhydroxylamine

Kaneko, Tsuyoshi,Kubo, Kanji,Sakurai, Tadamitsu

, p. 2757 - 2774 (2007/10/03)

Most important property of compartmentalized liquids such as micelles is that they have an ability to concentrate guest molecules into relatively small effective volumes and then to promote the re-encounter of such molecules. This property also makes mice

The Photolysis of N,O-Diacyl-N-phenylhydroxylamines

Sakurai, Tadamitsu,Yamamoto, Hirofumi,Yamada, Shuichi,Inoue, Hiroyasu

, p. 1174 - 1181 (2007/10/02)

The photochemical decomposition of the title compounds yielded the rearrangement products derived from 1,3- and 1,5-aroyloxyl migrations in addition to the fragmentation products typical of the aroyloxyl and amido radicals, while only 1,3-aroyloxyl migration was observed on thermolysis.The results of crossover experiments indicate an intramolecular rearrangement, probably involving homolysis of the N-O bond in the excited states.Triplet quenching studies demonstrate that the rearrangement and fragmentation proceed exclusively via the first excited singlet state.No formation of the rearrangement products on triplet sensitization was expl ained on the basis of the spin multiplicity effects on a radical-radical recombination process within a solvent cage.

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