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312305-59-2

4,6-dimethoxy-2-formyl-benzoic acid (1-methyl-7-oxo-heptyl) ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 312305-59-2 Structure

  • Basic information

    1. Product Name: 4,6-dimethoxy-2-formyl-benzoic acid (1-methyl-7-oxo-heptyl) ester
    2. Synonyms: 4,6-dimethoxy-2-formyl-benzoic acid (1-methyl-7-oxo-heptyl) ester
    3. CAS NO:312305-59-2
    4. Molecular Formula:
    5. Molecular Weight: 336.385
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 312305-59-2.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: 4,6-dimethoxy-2-formyl-benzoic acid (1-methyl-7-oxo-heptyl) ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4,6-dimethoxy-2-formyl-benzoic acid (1-methyl-7-oxo-heptyl) ester(312305-59-2)
    11. EPA Substance Registry System: 4,6-dimethoxy-2-formyl-benzoic acid (1-methyl-7-oxo-heptyl) ester(312305-59-2)

  • 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: 312305-59-2(Hazardous Substances Data)

312305-59-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 312305-59-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,2,3,0 and 5 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 312305-59:
(8*3)+(7*1)+(6*2)+(5*3)+(4*0)+(3*5)+(2*5)+(1*9)=92
92 % 10 = 2
So 312305-59-2 is a valid CAS Registry Number.

312305-59-2Downstream Products

312305-59-2Relevant articles and documents

Total syntheses of (S)-(-)-zearalenone and lasiodiplodin reveal superior metathesis activity of ruthenium carbene complexes with imidazol-2-ylidene ligands

Furstner,Thiel,Kindler,Bartkowska

, p. 7990 - 7995 (2007/10/03)

Total syntheses of the bioactive orsellinic acid derivatives zearalenone 3 and lasiodiplodin 1 are reported based on a ring-closing metathesis (RCM) reaction of styrene precursors as the key steps. These and closely related macrocyclizations are catalyzed

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