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217965-54-3

Ethyl 2-(azepan-2-yl)acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 217965-54-3 Structure

  • Basic information

    1. Product Name: Ethyl 2-(azepan-2-yl)acetate
    2. Synonyms: Ethyl 2-(azepan-2-yl)acetate
    3. CAS NO:217965-54-3
    4. Molecular Formula: C10H19NO2
    5. Molecular Weight: 185.26336
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 217965-54-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Ethyl 2-(azepan-2-yl)acetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: Ethyl 2-(azepan-2-yl)acetate(217965-54-3)
    11. EPA Substance Registry System: Ethyl 2-(azepan-2-yl)acetate(217965-54-3)

  • 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: 217965-54-3(Hazardous Substances Data)

217965-54-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 217965-54-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,7,9,6 and 5 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 217965-54:
(8*2)+(7*1)+(6*7)+(5*9)+(4*6)+(3*5)+(2*5)+(1*4)=163
163 % 10 = 3
So 217965-54-3 is a valid CAS Registry Number.

217965-54-3Downstream Products

217965-54-3Relevant articles and documents

α-C-H Bond Functionalization of Unprotected Alicyclic Amines: Lewis-Acid-Promoted Addition of Enolates to Transient Imines

Kim, Jae Hyun,Paul, Anirudra,Ghiviriga, Ion,Seidel, Daniel

, p. 797 - 801 (2021/02/06)

Enolizable cyclic imines, obtained in situ from their corresponding lithium amides by oxidation with simple ketone oxidants, are readily alkylated with a range of enolates to provide mono- and polycyclic β-aminoketones in a single operation, including the natural product (±)-myrtine. Nitrile anions also serve as competent nucleophiles in these transformations, which are promoted by BF3 etherate. β-Aminoesters derived from ester enolates can be converted to the corresponding β-lactams.

Ring constrained analogues of β-alanine-containing GPIIb/IIIa receptor antagonists

Sielecki, Thais M.,Wityak, John,Liu, Jie,Mousa, Shaker A.,Thoolen, Martin,Wexler, Ruth R.,Olson, Richard E.

, p. 449 - 452 (2007/10/03)

A series of ring constrained analogues of the GPIIb/IIIa receptor antagonist XR299 (1) was investigated as potential inhibitors of glycoprotein IIb/IIIa, a platelet receptor that plays a key role in platelet aggregation and platelet adhesion. Ring size was found to have a large effect on in vitro potency. Selected compounds showed good in vitro activity, a preference for binding to activated platelets, and modest duration of action when dosed iv as a racemate in a canine model. (C) 2000 DuPont Pharmaceuticals Company. Published by Elsevier Science Ltd. All rights reserved.

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