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1383783-12-7

C24H28O2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1383783-12-7 Structure

  • Basic information

    1. Product Name: C24H28O2
    2. Synonyms: C24H28O2
    3. CAS NO:1383783-12-7
    4. Molecular Formula:
    5. Molecular Weight: 348.485
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1383783-12-7.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: C24H28O2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C24H28O2(1383783-12-7)
    11. EPA Substance Registry System: C24H28O2(1383783-12-7)

  • 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: 1383783-12-7(Hazardous Substances Data)

1383783-12-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1383783-12-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,3,7,8 and 3 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1383783-12:
(9*1)+(8*3)+(7*8)+(6*3)+(5*7)+(4*8)+(3*3)+(2*1)+(1*2)=187
187 % 10 = 7
So 1383783-12-7 is a valid CAS Registry Number.

1383783-12-7Downstream Products

1383783-12-7Relevant articles and documents

Stereochemistry of hydroxylation of some chiral spiro-[2,5]octan-4-ones

Gella,Drushlyak,Pivnenko,Zubatyuk,Turov,Konovalova,Novikova,Shishkin

experimental part, p. 120 - 129 (2012/07/14)

Stereoselective oxidative alpha hydroxylation of (1R,5R,8R,3R)-1-aryl-5- isopropyl-8-methyl-3-spiro-[2,5]octan-4-ones has been found as a secondary process in the cyclopropanation of 2-arylidene isomenthanones with trimethylsulfoxonium iodide in DMSO/NaOH or DMF/NaOH system. Three stereoisomeric hydroxy ketones have been isolated from a reaction mixture of cyclopropanation reaction, but the reaction of oxidation carried out with isolated spiro-[2,5]octan-4-ones was stereoselective. The advantages of this method of stereoselective hydroxylation are room temperature of reaction and absence of expensive catalysts. The reduction of obtained hydroxy ketones was also stereoselective and gave the only trans-(4R,5S)-dioles. The structures have been confirmed with 1D and 2D 1H and 13C NMR, MS spectra and for stereoisomeric hydroxy ketones with X-ray analysis also.

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