Welcome to LookChem.com Sign In|Join Free

CAS

  • or

220063-63-8

2-(1-Hydroxy-2-phenyl-ethyl)-6-methoxy-phenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

220063-63-8 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 220063-63-8 Structure

  • Basic information

    1. Product Name: 2-(1-Hydroxy-2-phenyl-ethyl)-6-methoxy-phenol
    2. Synonyms: 2-(1-Hydroxy-2-phenyl-ethyl)-6-methoxy-phenol
    3. CAS NO:220063-63-8
    4. Molecular Formula:
    5. Molecular Weight: 244.29
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 220063-63-8.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-(1-Hydroxy-2-phenyl-ethyl)-6-methoxy-phenol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(1-Hydroxy-2-phenyl-ethyl)-6-methoxy-phenol(220063-63-8)
    11. EPA Substance Registry System: 2-(1-Hydroxy-2-phenyl-ethyl)-6-methoxy-phenol(220063-63-8)

  • 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: 220063-63-8(Hazardous Substances Data)

220063-63-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 220063-63-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,0,0,6 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 220063-63:
(8*2)+(7*2)+(6*0)+(5*0)+(4*6)+(3*3)+(2*6)+(1*3)=78
78 % 10 = 8
So 220063-63-8 is a valid CAS Registry Number.

220063-63-8Relevant articles and documents

Silver catalyzed zinc Barbier reaction of benzylic halides in water

Bieber, Lothar W.,Storch, Elisabeth C.,Malvestiti, Ivani,Da Silva, Margarete F.

, p. 9393 - 9396 (1998)

Benzylic chlorides react in aqueous dibasic potassium phosphate under silver catalysis with aromatic aldehydes in the presence of zinc dust to give 1,2-diaryl alcohols in moderate to good yields. Dimerization to bibenzyls and reduction of the halide are important side reactions. A wide range of substituted aromatic and heteroaromatic aldehydes and of substituted benzylic chlorides can be used. Aliphatic aldehydes and ketones are unreactive. A mechanism of two SET on the metal surface is discussed.

Substituted (ω-aminoalkoxy)stilbene derivatives as a new class of anticonvulsants

Kikumoto,Tobe,Fukami,Ninomiya,Egawa

, p. 645 - 649 (2007/10/02)

A series of substituted (ω-aminoalkoxy)stilbene derivatives has been synthesized and screened for anticonvulsant activity. The effect of structural modification of these molecules on the activities has been systematically examined. Potent anticonvulsant activity was displayed by 2-[4-(4-methyl-1-piperazinyl)butoxy]stilbene and some 2-[4-(3-alkoxy-1-piperidino)butoxy]stilbene derivatives, as determined by maximal electroshock seizure (MES) and pentylenetetrazol-induced convulsion tests in mice. One of these derivatives exhibited more potent anti-MES activity than diphenylhydantoin and carbamazepine in further pharmacological tests in rats, and its therapeutic index was superior to those of two antiepileptic drugs.

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 220063-63-8