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1056683-09-0

C18H21NO3 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1056683-09-0 Structure

  • Basic information

    1. Product Name: C18H21NO3
    2. Synonyms: C18H21NO3
    3. CAS NO:1056683-09-0
    4. Molecular Formula:
    5. Molecular Weight: 299.37
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1056683-09-0.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: C18H21NO3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C18H21NO3(1056683-09-0)
    11. EPA Substance Registry System: C18H21NO3(1056683-09-0)

  • 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: 1056683-09-0(Hazardous Substances Data)

1056683-09-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1056683-09-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,5,6,6,8 and 3 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1056683-09:
(9*1)+(8*0)+(7*5)+(6*6)+(5*6)+(4*8)+(3*3)+(2*0)+(1*9)=160
160 % 10 = 0
So 1056683-09-0 is a valid CAS Registry Number.

1056683-09-0Downstream Products

1056683-09-0Relevant articles and documents

Novel 2,4-methanoadamantane-benzazepine by domino photochemistry of N-(1-adamantyl)phthalimide

Basaric, Nikola,Horvat, Margareta,Mlinaric-Majerski, Kata,Zimmermann, Elmar,Neudoerfl, Joerg,Griesbeck, Axel G.

, p. 3965 - 3968 (2008)

(Chemical Equation Presented) The photochemical reaction of N-(1-adamantyl)phthalimide (1) gives cleanly one product, the novel hexacyclic benzazepine derivative of 2,4-methanoadamantane 2. Its structure was characterized by spectroscopic methods and X-ray analysis and represent the first example of the 2-azahexacyclo[8.7.1.11,4.04,9.0 11,16.012,18]nonadeca-4,6,8-triene skeleton. The product is formed by a domino process of two consecutive excited-state intramolecular γ-hydrogen-transfer reactions. Base hydrolysis of the benzazepine 2 gives in high yield the keto derivative of the 1,2-substituted adamantane ε-amino acid 3.

Antiproliferative and antiviral activity of three libraries of adamantane derivatives

Basaric, Nikola,Sohora, Margareta,Cindro, Nikola,Mlinaric-Majerski, Kata,De Clercq, Erik,Balzarini, Jan

, p. 334 - 340 (2014/05/20)

Three libraries of adamantane derivatives were synthesized and evaluated for antiviral and antiproliferative activities against a broad variety of DNA and RNA viruses. Whereas none of the compounds exhibit antiviral activity at subtoxic concentrations, antiproliferative activity was found against murine leukemia cells (L1210), human T-lymphocyte cells (CEM), and cervix carcinoma cells (HeLa) for 4, 8, and 10.

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