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Benzeneacetic acid, a-[(4-hydroxyphenyl)thio]-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 287393-39-9 Structure
  • Basic information

    1. Product Name: Benzeneacetic acid, a-[(4-hydroxyphenyl)thio]-, ethyl ester
    2. Synonyms:
    3. CAS NO:287393-39-9
    4. Molecular Formula: C16H16O3S
    5. Molecular Weight: 288.367
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 287393-39-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Benzeneacetic acid, a-[(4-hydroxyphenyl)thio]-, ethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzeneacetic acid, a-[(4-hydroxyphenyl)thio]-, ethyl ester(287393-39-9)
    11. EPA Substance Registry System: Benzeneacetic acid, a-[(4-hydroxyphenyl)thio]-, ethyl ester(287393-39-9)
  • 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: 287393-39-9(Hazardous Substances Data)

287393-39-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 287393-39-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,7,3,9 and 3 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 287393-39:
(8*2)+(7*8)+(6*7)+(5*3)+(4*9)+(3*3)+(2*3)+(1*9)=189
189 % 10 = 9
So 287393-39-9 is a valid CAS Registry Number.

287393-39-9Relevant articles and documents

Palladium-Catalyzed Synthesis of Bis-Substituted Sulfoxonium Ylides

Janot, Christopher,Palamini, Pierre,Dobson, Benjamin C.,Muir, James,A?ssa, Christophe

, p. 296 - 299 (2019)

The lack of general access to bis-substituted sulfoxonium ylides is addressed by developing a palladium-catalyzed C-H cross-coupling of α-ester sulfoxonium ylides with (hetero)aryl iodides, bromides, and triflates. Three different catalysts have been eval

Synthesis and structure-activity relationships of 4-alkynyloxy phenyl sulfanyl, sulfinyl, and sulfonyl alkyl hydroxamates as tumor necrosis factor-α converting enzyme and matrix metalloproteinase inhibitors

Venkatesan, Aranapakam M.,Davis, Jamie M.,Grosu, George T.,Baker, Jannie,Zask, Arie,Levin, Jeremy I.,Ellingboe, John,Skotnicki, Jerauld S.,DiJoseph, John F.,Sung, Amy,Jin, Guixian,Xu, Weixin,McCarthy, Diane Joseph,Barone, Dauphine

, p. 6255 - 6269 (2007/10/03)

A series of 4-alkynyloxy phenyl sulfanyl, sulfinyl and sulfony alkyl and piperidine-4-carboxylic acid hydroxamides were synthesized. Their structure-activity relationships, against tumor necrosis factor-α (TACE) and matrix metalloproteinase (MMP) inhibito

Alkynyl containing hydroxamic acid compounds as matrix metalloproteinase and tace inhibitors

-

Page column 62, (2008/06/13)

Compounds of the formula are useful in treating disease conditions mediated by TNF-α, such as rheumatoid arthritis, osteoarthritis, sepsis, AIDS, ulcerative colitis, multiple sclerosis, Crohn's disease and degenerative cartilage loss.

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