Welcome to LookChem.com Sign In|Join Free

CAS

  • or

97715-60-1

4-hydroxy-5-phenoxy-4-methyl-1-pentene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

97715-60-1 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 97715-60-1 Structure

  • Basic information

    1. Product Name: 4-hydroxy-5-phenoxy-4-methyl-1-pentene
    2. Synonyms: 4-hydroxy-5-phenoxy-4-methyl-1-pentene
    3. CAS NO:97715-60-1
    4. Molecular Formula:
    5. Molecular Weight: 192.258
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 97715-60-1.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: 4-hydroxy-5-phenoxy-4-methyl-1-pentene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-hydroxy-5-phenoxy-4-methyl-1-pentene(97715-60-1)
    11. EPA Substance Registry System: 4-hydroxy-5-phenoxy-4-methyl-1-pentene(97715-60-1)

  • 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: 97715-60-1(Hazardous Substances Data)

97715-60-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97715-60-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,7,1 and 5 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 97715-60:
(7*9)+(6*7)+(5*7)+(4*1)+(3*5)+(2*6)+(1*0)=171
171 % 10 = 1
So 97715-60-1 is a valid CAS Registry Number.

97715-60-1Downstream Products

97715-60-1Relevant articles and documents

Ti/Ni-based multimetallic system for the efficient allylation of carbonyl compounds

Martinez-Peragon, Angela,Millan, Alba,Campana, Araceli G.,Rodriguez-Marquez, Irene,Resa, Sandra,Miguel, Delia,Alvarez De Cienfuegos, Luis,Cuerva, Juan M.

, p. 1499 - 1503 (2012)

A mild method for the allylation of carbonyl compounds is presented. This methodology allows the allylation of a broad range of carbonyl compounds starting with allyl carbonates as pronucleophiles. Noteworthy is that ketones, infrequent substrates in other related protocols, are suitable substrates under these reaction conditions. Moreover, the reaction proceeds at room temperature with the use of catalytic amounts of both Ni and Ti catalysts. The success of this strategy is based on the perfect match between the late transition metal (nickel) and the radical reagent (titanium). The use of Ni instead of Pd widens the scope of this transformation and makes this method more economical.

PROSTANOIDS. XIII. SYNTHESIS OF THE 15- AND 16-METHYL DERIVATIVES OF THE ω-PHENOXY ANALOGS OF 11-DEOXYPROSTAGLANDINS E1

Tolstikov, G. A.,Miftakhov, M. S.,Danilova, N. A.,Shitikova, O. V.

, p. 74 - 80 (2007/10/02)

(+/-)-11-Deoxy-16-phenoxy-15-methyl-ω-tetranorprostaglandin E1 and 11,15-dideoxy-16-hydroxy-17-phenoxy-16-methyl-ω-trinor-α-homoprostaglandin E1 were synthesized by the 1,4-conjugate addition of the cuprate rea

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 97715-60-1