Welcome to LookChem.com Sign In|Join Free

CAS

  • or

52708-30-2

3-methoxycyclohex-3-ene carbonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

52708-30-2 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 52708-30-2 Structure

  • Basic information

    1. Product Name: 3-methoxycyclohex-3-ene carbonitrile
    2. Synonyms:
    3. CAS NO:52708-30-2
    4. Molecular Formula:
    5. Molecular Weight: 137.181
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 52708-30-2.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: 3-methoxycyclohex-3-ene carbonitrile(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-methoxycyclohex-3-ene carbonitrile(52708-30-2)
    11. EPA Substance Registry System: 3-methoxycyclohex-3-ene carbonitrile(52708-30-2)

  • 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: 52708-30-2(Hazardous Substances Data)

52708-30-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52708-30-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,7,0 and 8 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 52708-30:
(7*5)+(6*2)+(5*7)+(4*0)+(3*8)+(2*3)+(1*0)=112
112 % 10 = 2
So 52708-30-2 is a valid CAS Registry Number.

52708-30-2Downstream Products

52708-30-2Relevant articles and documents

Further studies of intramolecular michael reactions of nitrosoalkenes for construction of functionalized bridged ring systems

Kumar, Praveen,Li, Puhui,Korboukh, Ilia,Wang, Tony L.,Yennawar, Hemant,Weinreb, Steven M.

, p. 2094 - 2101 (2011)

A wide variety of stabilized carbanions have been found to participate as nucleophiles in intramolecular Michael-type conjugate additions to in situ generated nitrosoalkenes to form bridged carbocyclic systems. The vinylnitroso platforms for these cyclizations have been prepared via two key steps involving ring-closing metathesis of vinyl chlorides and regioselective conversion of vinyl chlorides to α-chloroketones with sodium hypochlorite in glacial acetic acid/acetone. An alternative approach to preparation of some cyclization substrates has involved use of more reactive enol ethers as precursors to the requisite α-chloroketones. A sulfonamide anion has also been found to be an effective nucleophile in this type of reaction, leading to formation of a 6-azabicyclo[3.2.1]octane.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 52708-30-2