Welcome to LookChem.com Sign In|Join Free

CAS

  • or

74203-25-1

1-(1-Phenyl-allyl)-adamantane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

74203-25-1 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 74203-25-1 Structure

  • Basic information

    1. Product Name: 1-(1-Phenyl-allyl)-adamantane
    2. Synonyms: 1-(1-Phenyl-allyl)-adamantane
    3. CAS NO:74203-25-1
    4. Molecular Formula:
    5. Molecular Weight: 252.4
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 74203-25-1.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: 1-(1-Phenyl-allyl)-adamantane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(1-Phenyl-allyl)-adamantane(74203-25-1)
    11. EPA Substance Registry System: 1-(1-Phenyl-allyl)-adamantane(74203-25-1)

  • 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: 74203-25-1(Hazardous Substances Data)

74203-25-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74203-25-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,2,0 and 3 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 74203-25:
(7*7)+(6*4)+(5*2)+(4*0)+(3*3)+(2*2)+(1*5)=101
101 % 10 = 1
So 74203-25-1 is a valid CAS Registry Number.

74203-25-1Downstream Products

74203-25-1Relevant articles and documents

Synthesis of Adamantane Derivatives. 49. Substitution Reaction of 1-Adamantyl Chloride with Some Trimethylsilylated Unsaturated Compounds

Sasaki, Tadashi,Usuki, Arimitsu,Ohno, Masatomi

, p. 3559 - 3564 (1980)

Catalytic substitution reactions at the adamantane bridgehead were studied by using α,β- and β,γ-unsaturated trimethylsilanes.Treatment of 1-adamantyl (Ad) chloride (1) with allyltrimethylsilane and its heteroanalogues, X=Y-Z-SiMe3, in the presence of Lewis acid as a catalyst gave the products Ad-X-Y=Z, X=Y+(Ad)-Z-, and X=Y-Z-Ad, depending on the attack site of the adamantyl group on each X, Y, and Z atom.Treatment of 1 with (phenylethynyl)trimethylsilane also gave a substituted adamantane in good yield.The substitution reactions of 1 with aryl- and heteroaryltrimethylsilanes under similar conditions occurred at a position distinct from that of acetylation, indicating that adamantylation was not influenced by an electronic effect of the trimethylsilyl group.

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 74203-25-1