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  • 1333699-07-2 Structure
  • Basic information

    1. Product Name: C18H23FN2O3
    2. Synonyms:
    3. CAS NO:1333699-07-2
    4. Molecular Formula:
    5. Molecular Weight: 334.391
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1333699-07-2.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: C18H23FN2O3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C18H23FN2O3(1333699-07-2)
    11. EPA Substance Registry System: C18H23FN2O3(1333699-07-2)
  • 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: 1333699-07-2(Hazardous Substances Data)

1333699-07-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1333699-07-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,3,6,9 and 9 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1333699-07:
(9*1)+(8*3)+(7*3)+(6*3)+(5*6)+(4*9)+(3*9)+(2*0)+(1*7)=172
172 % 10 = 2
So 1333699-07-2 is a valid CAS Registry Number.

1333699-07-2Downstream Products

1333699-07-2Relevant articles and documents

Toward lead-oriented synthesis: One-pot version of castagnoli condensation with nonactivated alicyclic anhydrides

Ryabukhin, Sergey V.,Panov, Dmitriy M.,Granat, Dmitry S.,Ostapchuk, Eugeniy N.,Kryvoruchko, Dmitriy V.,Grygorenko, Oleksandr O.

, p. 146 - 153 (2014/04/03)

One-pot variation of Castagnoli condensation, that is, reaction of cyclic anhydrides, amines, and aldehydes, has been developed as a combinatorial approach to 1,2-disubstituted 5-oxopyrrolidine- and 6-oxopiperidine-3-carboxylic acids, as well as their benzo-analogues. Utility of the method to multigram preparation of building blocks and synthetic intermediates was also demonstrated. The final products are obtained in high yields and diastereoselectivity. The method fits well in the concept of lead-oriented synthesis; in particular, it can be used for the design of lead-like compound libraries, even if the strictest cut-offs are applied to the physicochemical properties of their members.

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