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CAS

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1464782-05-5

C21H33NO5 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1464782-05-5 Structure

  • Basic information

    1. Product Name: C21H33NO5
    2. Synonyms: C21H33NO5
    3. CAS NO:1464782-05-5
    4. Molecular Formula:
    5. Molecular Weight: 379.497
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1464782-05-5.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: C21H33NO5(CAS DataBase Reference)
    10. NIST Chemistry Reference: C21H33NO5(1464782-05-5)
    11. EPA Substance Registry System: C21H33NO5(1464782-05-5)

  • 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: 1464782-05-5(Hazardous Substances Data)

1464782-05-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1464782-05-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,6,4,7,8 and 2 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1464782-05:
(9*1)+(8*4)+(7*6)+(6*4)+(5*7)+(4*8)+(3*2)+(2*0)+(1*5)=185
185 % 10 = 5
So 1464782-05-5 is a valid CAS Registry Number.

1464782-05-5Relevant articles and documents

Asymmetric formation of tert-alkylamines from serinols by a dual function catalyst

You, Young Suk,Kim, Tae Woo,Kang, Sung Ho

supporting information, p. 9669 - 9671 (2013/10/08)

Consecutive intramolecular desymmetrization and kinetic resolution of 2-substituted N-phenoxycarbonylserinols have been achieved in one-pot by a single chiral catalyst, bisox(7)-CuCl2, to form oxazolidinones with remarkable enantioselectivities (94-99% ee) as tert-alkylamine building blocks. The process culminates in a dual-function of the chiral catalyst. The Royal Society of Chemistry 2013.

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