Welcome to LookChem.com Sign In|Join Free

CAS

  • or

92975-49-0

2-Pentenoic acid, 5-phenyl-3-[(trimethylsilyl)oxy]-, ethyl ester, (Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

92975-49-0 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 92975-49-0 Structure

  • Basic information

    1. Product Name: 2-Pentenoic acid, 5-phenyl-3-[(trimethylsilyl)oxy]-, ethyl ester, (Z)-
    2. Synonyms:
    3. CAS NO:92975-49-0
    4. Molecular Formula: C16H24O3Si
    5. Molecular Weight: 292.45
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 92975-49-0.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: 2-Pentenoic acid, 5-phenyl-3-[(trimethylsilyl)oxy]-, ethyl ester, (Z)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Pentenoic acid, 5-phenyl-3-[(trimethylsilyl)oxy]-, ethyl ester, (Z)-(92975-49-0)
    11. EPA Substance Registry System: 2-Pentenoic acid, 5-phenyl-3-[(trimethylsilyl)oxy]-, ethyl ester, (Z)-(92975-49-0)

  • 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: 92975-49-0(Hazardous Substances Data)

92975-49-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92975-49-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,9,7 and 5 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 92975-49:
(7*9)+(6*2)+(5*9)+(4*7)+(3*5)+(2*4)+(1*9)=180
180 % 10 = 0
So 92975-49-0 is a valid CAS Registry Number.

92975-49-0Relevant articles and documents

Enantioselective N-Heterocyclic Carbene Catalysis via the Dienyl Acyl Azolium

Gillard, Rachel M.,Fernando, Jared E. M.,Lupton, David W.

, p. 4712 - 4716 (2018)

Herein we report the enantioselective N-heterocyclic carbene catalyzed (4+2) annulation of the dienyl acyl azolium with enolates. The reaction exploits readily accessible acyl fluorides and TMS enol ethers to give a range of highly enantio- and diastereo-enriched cyclohexenes (most >97:3 er and >20:1 dr). The reaction was found to require high nucleophilicity NHC catalysts with mechanistic studies supporting a stepwise 1,6-addition/β-lactonization.

Domino reaction of 1,3-bis(trimethylsilyloxy)-1,3-dienes with oxalyl chloride: General and stereoselective synthesis of γ-alkylidenebutenolides

Langer, Peter,Schneider, Toni,Stoll, Martin

, p. 3204 - 3214 (2007/10/03)

The Lewis acid catalyzed cyclization of oxalyl chloride with 1,3-bis-(trimethylsilyloxy)-1,3-dienes 3, derived from 1,3-dicarbonyl compounds 1, provides a new and general approach for the synthesis of γ-alkylidenebutenolides 4, a pharmacologically and syn

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 92975-49-0