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5-(naphthalen-1-yl)benzene-1,3-diol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 881888-23-9 Structure
  • Basic information

    1. Product Name: 5-(naphthalen-1-yl)benzene-1,3-diol
    2. Synonyms: 5-(naphthalen-1-yl)benzene-1,3-diol
    3. CAS NO:881888-23-9
    4. Molecular Formula:
    5. Molecular Weight: 236.27
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 881888-23-9.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: 5-(naphthalen-1-yl)benzene-1,3-diol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-(naphthalen-1-yl)benzene-1,3-diol(881888-23-9)
    11. EPA Substance Registry System: 5-(naphthalen-1-yl)benzene-1,3-diol(881888-23-9)
  • 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: 881888-23-9(Hazardous Substances Data)

881888-23-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 881888-23-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,1,8,8 and 8 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 881888-23:
(8*8)+(7*8)+(6*1)+(5*8)+(4*8)+(3*8)+(2*2)+(1*3)=229
229 % 10 = 9
So 881888-23-9 is a valid CAS Registry Number.

881888-23-9Relevant articles and documents

Chiral Dinuclear Vanadium Complex-Mediated Oxidative Coupling of Resorcinols

Sako, Makoto,Aoki, Takanori,Zumbr?gel, Nadine,Schober, Lukas,Gr?ger, Harald,Takizawa, Shinobu,Sasai, Hiroaki

, p. 1580 - 1587 (2019/02/08)

A method for the highly regio- and enantioselective oxidative coupling of resorcinols has been established by using dibrominated dinuclear vanadium(V) catalyst 1c under air. When resorcinols bearing an aryl substituent were applied as substrates to the co

Structural modifications of the cannabinoid side chain towards C3-aryl and 1′,1′-cycloalkyl-1′-cyano cannabinoids

Papahatjis, Demetris P.,Nahmias, Victoria R.,Andreou, Thanos,Fan, Pusheng,Makriyannis, Alexandros

, p. 1616 - 1620 (2007/10/03)

The compounds reported in this study are Δ8-THC analogues in which the C3 five-carbon linear side chain of Δ8-THC was replaced with aryl and 1′,1′-cycloalkyl substituents. Of the compounds described here analogues 2d (CB1,

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