Welcome to LookChem.com Sign In|Join Free

CAS

  • or
Morpholine, 3-methoxy-4-(phenylacetyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

92912-55-5 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 92912-55-5 Structure
  • Basic information

    1. Product Name: Morpholine, 3-methoxy-4-(phenylacetyl)-
    2. Synonyms:
    3. CAS NO:92912-55-5
    4. Molecular Formula: C13H17NO3
    5. Molecular Weight: 235.283
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 92912-55-5.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: Morpholine, 3-methoxy-4-(phenylacetyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Morpholine, 3-methoxy-4-(phenylacetyl)-(92912-55-5)
    11. EPA Substance Registry System: Morpholine, 3-methoxy-4-(phenylacetyl)-(92912-55-5)
  • 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: 92912-55-5(Hazardous Substances Data)

92912-55-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92912-55-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,9,1 and 2 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 92912-55:
(7*9)+(6*2)+(5*9)+(4*1)+(3*2)+(2*5)+(1*5)=145
145 % 10 = 5
So 92912-55-5 is a valid CAS Registry Number.

92912-55-5Downstream Products

92912-55-5Relevant articles and documents

Electro-organic Reactions. Part 23. Regioselectivity and the Stereochemistry of Anodic Methoxylation of N-Acylpiperidines and N-Acylmorpholines

Palasz, Peter D.,Utley, James H. P.,Hardstone, J. David

, p. 807 - 814 (2007/10/02)

Anodic methoxylation of conformationally biassed N-acylpiperidines has been shown to give axial substitution due to steric constraints imposed by relatively slow rotation of the planar N-acyl groups.These steric constraints also account for the regioselec

Electro-organic Reactions. Part 22. An Entry into the Quinolizidine and Benzoquinolizidine Ring Systems via Anodic Methoxylation

Palasz, Peter D.,Utley, James H. P.,Hardstone, J. David

, p. 281 - 292 (2007/10/02)

Examples of the quinolizidine and benzoquinolizidine ring systems (1,1-bisethoxycarbonyl-4-oxo-quinolizidine, 1,3,4,6,7,11b-hexahydro-2H-benzoquinolizidine, and 1,2-t-butyl-3,4,6,7,11b-hexahydro-2H-benzo-quinolizidine) have been synthesized by routes which involve initial anodic methoxylation of piperidine precursors with subsequent intramolecular Lewis acid-catalysed cyclisation reactions.Reaction conditions for such cyclisations have been explored; success depends on a correct choice of catalyst (usually aluminium chloride) and, critically, on steric factors.The stereochemistry of the cyclic products has been established and the stereochemical course of the reactions is commented upon.

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 92912-55-5