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4-(2',3',4',5'-Tetramethoxy-6'-methylphenyl)-4-oxobutyric acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 292820-05-4 Structure
  • Basic information

    1. Product Name: 4-(2',3',4',5'-Tetramethoxy-6'-methylphenyl)-4-oxobutyric acid
    2. Synonyms: 4-(2',3',4',5'-Tetramethoxy-6'-methylphenyl)-4-oxobutyric acid
    3. CAS NO:292820-05-4
    4. Molecular Formula:
    5. Molecular Weight: 312.32
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 292820-05-4.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: 4-(2',3',4',5'-Tetramethoxy-6'-methylphenyl)-4-oxobutyric acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(2',3',4',5'-Tetramethoxy-6'-methylphenyl)-4-oxobutyric acid(292820-05-4)
    11. EPA Substance Registry System: 4-(2',3',4',5'-Tetramethoxy-6'-methylphenyl)-4-oxobutyric acid(292820-05-4)
  • 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: 292820-05-4(Hazardous Substances Data)

292820-05-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 292820-05-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,2,8,2 and 0 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 292820-05:
(8*2)+(7*9)+(6*2)+(5*8)+(4*2)+(3*0)+(2*0)+(1*5)=144
144 % 10 = 4
So 292820-05-4 is a valid CAS Registry Number.

292820-05-4Relevant articles and documents

Quinone - Annonaceous acetogenins: Synthesis and complex I inhibition studies of a new class of natural product hybrids

Arndt, Sabine,Emde, Ulrich,Baeurle, Stefan,Friedrich, Thorsten,Grubert, Lutz,Koert, Ulrich

, p. 993 - 1005 (2001)

The natural product hybrids quinone-mucocin and quinone- squamocin D were synthesized. In these hybrids, the butenolide unit of the annonaceous acetogenins mucocin and squamocin D is exchanged for the quinone moiety of the natural complex I substrate ubiq

Natural-product hybrids: Design, synthesis, and biological evaluation of quinone - Annonaceous acetogenins

Hoppen, Sabine,Emde, Ulrich,Friedrich, Thorsten,Grubert, Lutz,Koert, Ulrich

, p. 2099 - 2102 (2007/10/03)

Replacement of the butyrolactone unit of the natural products with a quinone subunit has resulted in the synthesis of natural-product hybrids of quinone-mucocin (1). These compounds, which are combined from partial structures of annonaceous acetogenins an

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