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CAS

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171808-02-9

METHYL 4'-TOSYLMYCOPHENOLATE, with the CAS number 171808-02-9, is a compound that is primarily utilized in the field of organic synthesis. It is characterized by its clear oil chemical properties, making it a versatile and valuable component in various chemical reactions and processes.

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  • 171808-02-9 Structure

  • Basic information

    1. Product Name: METHYL 4'-TOSYLMYCOPHENOLATE
    2. Synonyms: METHYL 4'-TOSYLMYCOPHENOLATE;(4E)-6-[1,3-Dihydro-6-Methoxy-7-Methyl-4-[[(4-Methylphenyl)sulfonyl]oxy]-3-oxo-5-isobenzofuranyl]-4-Methyl-4-hexenoic Acid Methyl Ester;UEHFBCOBVAUDFJ-LZYBPNLTSA-N
    3. CAS NO:171808-02-9
    4. Molecular Formula: C25H28O8S
    5. Molecular Weight: 488.55002
    6. EINECS: N/A
    7. Product Categories: Aromatics;Intermediates & Fine Chemicals;Pharmaceuticals
    8. Mol File: 171808-02-9.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: Dichloromethane
    9. CAS DataBase Reference: METHYL 4'-TOSYLMYCOPHENOLATE(CAS DataBase Reference)
    10. NIST Chemistry Reference: METHYL 4'-TOSYLMYCOPHENOLATE(171808-02-9)
    11. EPA Substance Registry System: METHYL 4'-TOSYLMYCOPHENOLATE(171808-02-9)

  • 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: 171808-02-9(Hazardous Substances Data)

171808-02-9 Usage

Uses

Used in Organic Synthesis:
METHYL 4'-TOSYLMYCOPHENOLATE is used as a synthetic intermediate for the creation of various organic compounds. Its unique structure and reactivity allow it to be employed in a wide range of chemical reactions, facilitating the synthesis of complex molecules and contributing to the development of new materials and pharmaceuticals.
Used in Pharmaceutical Industry:
METHYL 4'-TOSYLMYCOPHENOLATE is used as a key component in the development of novel drugs and therapeutic agents. Its application in this industry is due to its potential to be incorporated into the molecular structure of various pharmaceutical compounds, enhancing their efficacy and targeting specific biological pathways.
Used in Chemical Research:
METHYL 4'-TOSYLMYCOPHENOLATE is also used as a research tool in the field of chemistry. Its unique properties and reactivity make it an ideal candidate for studying various chemical reactions and mechanisms, furthering our understanding of organic chemistry and its applications.

Check Digit Verification of cas no

The CAS Registry Mumber 171808-02-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,1,8,0 and 8 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 171808-02:
(8*1)+(7*7)+(6*1)+(5*8)+(4*0)+(3*8)+(2*0)+(1*2)=129
129 % 10 = 9
So 171808-02-9 is a valid CAS Registry Number.

171808-02-9Relevant articles and documents

Mycophenolic acid as a latent agonist of PPARγ

Ubukata, Makoto,Takamori, Hitomi,Ohashi, Misaki,Mitsuhashi, Shinya,Yamashita, Kaoru,Asada, Tomohisa,Nakajima, Noriyuki,Matsuura, Nobuyasu,Tsuruga, Mie,Taki, Keiko,Magae, Junji

, p. 4767 - 4770 (2007)

Mycophenolic acid (MPA), known as an inhibitor of inosine monophosphate dehydrogenase (IMPDH), was found to inhibit the differentiation of 3T3-L1 pre-adipocytes into mature adipocytes. Although the effect of MPA was attributed to inhibition of IMPDH, we u

Structure-activity relationships for inhibition of inosine monophosphate dehydrogenase by nuclear variants of mycophenolic acid

Nelson, Peter H.,Carr, Stephen F.,Devens, Bruce H.,Eugui, Elsie M.,Franco, Fidencio,Gonzalez, Carlos,Hawley, Ronald C.,Loughhead, David G.,Milan, David J.,Papp, Eva,Patterson, John W.,Rouhafza, Sussan,Sjogren, Eric B.,Smith, David B.,Stephenson, Rebecca A.,Talamas, Francisco X.,Waltos, Ann-Marie,Weikert, Robert J.,Wu, John C.

, p. 4181 - 4196 (2007/10/03)

Structure-activity relationships in the region of the phthalide ring of the inosine monophosphate dehydrogenase inhibitor mycophenolic acid have been explored. Replacement of the lactone ring with other cyclic moieties resulted in loss of potency, especia

Method of using 4-amino 6-substituted mycophenolic acid and derivatives

-

, (2008/06/13)

The disclosed derivatives of mycophenolic acid are therapeutic agents advantageous in the treatment of disease states indicated for mycophenolic acid and/or mycophenolate mofetil and other immunosuppressant agents.

6-substituted mycophenolic acid and derivatives

-

, (2008/06/13)

The disclosed 6-substituted derivatives of mycophenolic acid are therapeutic agents advantageous in the treatment of disease states indicated for mycophenolic acid and/or mycophenolate mofetil.

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