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29201-96-5

C27H28O9 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 29201-96-5 Structure

  • Basic information

    1. Product Name: C27H28O9
    2. Synonyms: C27H28O9
    3. CAS NO:29201-96-5
    4. Molecular Formula:
    5. Molecular Weight: 496.514
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 29201-96-5.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: C27H28O9(CAS DataBase Reference)
    10. NIST Chemistry Reference: C27H28O9(29201-96-5)
    11. EPA Substance Registry System: C27H28O9(29201-96-5)

  • 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: 29201-96-5(Hazardous Substances Data)

29201-96-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29201-96-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,2,0 and 1 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 29201-96:
(7*2)+(6*9)+(5*2)+(4*0)+(3*1)+(2*9)+(1*6)=105
105 % 10 = 5
So 29201-96-5 is a valid CAS Registry Number.

29201-96-5Relevant articles and documents

Practical Synthesis of Polymethylated Flavones: Nobiletin and Its Desmethyl Derivatives

Asakawa, Tomohiro,Sagara, Hiroto,Kanakogi, Masaki,Hiza, Aiki,Tsukaguchi, Yuta,Ogawa, Takahiro,Nakayama, Miho,Ouchi, Hitoshi,Inai, Makoto,Kan, Toshiyuki

, p. 595 - 602 (2019/04/01)

We present a practical synthesis of the polymethoxylated citrus flavone nobiletin that is suitable for use on a hundred gram scale. Ready availability of this compound and its derivatives will aid detailed chemical-biological investigations of their biological activities, including activation of signaling via the cAMP-dependent protein kinase A/extracellular signal-related protein kinase/cAMP response element-binding protein pathway.

Concise synthesis of polymethoxyflavone sudachitin and its derivatives, and biological evaluations

Sagara, Hiroto,Kanakogi, Masaki,Tara, Yuki,Ouchi, Hitoshi,Kimura, Junko,Kaneko, Yukiko,Inai, Makoto,Asakawa, Tomohiro,Ishikawa, Tomohisa,Kan, Toshiyuki

, p. 1816 - 1818 (2018/04/11)

We accomplished a divergent synthesis of sudachitin (2), a polymethoxyflavone isolated from citrus fruits, and six derivatives from acetophenone 9, which was an intermediate in our previous synthesis of nobiletin (1). Compound 2 enhanced glucose-induced i

Nobiletin metabolites: Synthesis and inhibitory activity against matrix metalloproteinase-9 production

Oshitari, Tetsuta,Okuyama, Yuji,Miyata, Yoshiki,Kosano, Hiroshi,Takahashi, Hideyo,Natsugari, Hideaki

, p. 4540 - 4544 (2011/09/12)

A divergent synthesis of nobiletin metabolites was developed through highly oxygenated acetophenone derivative. We used commercially available methyl 3,4,5-trimethoxybenzoate as a starting material for concise preparation of the key intermediate, 2′-hydro

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