Welcome to LookChem.com Sign In|Join Free

CAS

  • or

1111323-43-3

6-allylnaphthalen-2-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1111323-43-3 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 1111323-43-3 Structure

  • Basic information

    1. Product Name: 6-allylnaphthalen-2-ol
    2. Synonyms: 6-allylnaphthalen-2-ol
    3. CAS NO:1111323-43-3
    4. Molecular Formula:
    5. Molecular Weight: 184.238
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1111323-43-3.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: 6-allylnaphthalen-2-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-allylnaphthalen-2-ol(1111323-43-3)
    11. EPA Substance Registry System: 6-allylnaphthalen-2-ol(1111323-43-3)

  • 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: 1111323-43-3(Hazardous Substances Data)

1111323-43-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1111323-43-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,1,1,3,2 and 3 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1111323-43:
(9*1)+(8*1)+(7*1)+(6*1)+(5*3)+(4*2)+(3*3)+(2*4)+(1*3)=73
73 % 10 = 3
So 1111323-43-3 is a valid CAS Registry Number.

1111323-43-3Downstream Products

1111323-43-3Relevant articles and documents

Selective arylation, alkenylation, and cyclization of dibromonaphthols, using visible light, via carbene intermediates

Verga, Daniela,Doria, Filippo,Mella, Mariella,Freccero, Mauro

body text, p. 5311 - 5319 (2009/11/30)

(Chemical Equation Presented) The photoreactivity of several 3-substituted-1,6-dibromo-2-naphthols has been investigated in neat acetonitrile in the presence of diluted Et3N and in aqueous buffered acetonitrile (pH 8, phosphate buffered), using visible light (450 nm). Hydrobromic acid loss in the presence of the base, for the unsubstituted naphthol, or heterolytic C-Br cleavage directly from the naphtholates, for the more acid 3-substutited naphthols (R = COOCH3, CONH2, CONMe2), generates electrophilic carbene intermediates, which have been successfully trapped by molecular oxygen, pyrrole, acrylonitrile, ethyl vinyl ether, and allyltrimethylsilane. Product distribution analysis reveals three types of products arising from (i) arylation, (ii) alkenylation, and (iii) cyclization reactions. The generation and the reactivity of α-ketocarbene intermediates, as electrophilc diradicals, has been supported by laser flash photolysis, with the detection of both the carbene (λmax 510 nm) and 1,2-naphthoquinone-O-oxide (R = CONMe2, λ max 600 nm) in the presence of O2.

Photoarylation/alkylation of bromonaphthols

Pretali, Luca,Doria, Filippo,Verga, Daniela,Profumo, Antonella,Freccero, Mauro

experimental part, p. 1034 - 1041 (2009/07/04)

The photochemistry of 6-bromo-2-naphthols has been studied in acetonitrile, aqueous acetonitrile, and isopropyl alcohol in the absence and in the presence of triethylamine by product distribution analysis, laser flash photolysis (LFP), fluorescence, phosp

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 1111323-43-3