Welcome to LookChem.com Sign In|Join Free

CAS

  • or
4-(4-hydroxybutyl)benzonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

92367-55-0 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 92367-55-0 Structure
  • Basic information

    1. Product Name: 4-(4-hydroxybutyl)benzonitrile
    2. Synonyms: 4-(4-hydroxybutyl)benzonitrile
    3. CAS NO:92367-55-0
    4. Molecular Formula:
    5. Molecular Weight: 175.23
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 92367-55-0.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-(4-hydroxybutyl)benzonitrile(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(4-hydroxybutyl)benzonitrile(92367-55-0)
    11. EPA Substance Registry System: 4-(4-hydroxybutyl)benzonitrile(92367-55-0)
  • 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: 92367-55-0(Hazardous Substances Data)

92367-55-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92367-55-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,3,6 and 7 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 92367-55:
(7*9)+(6*2)+(5*3)+(4*6)+(3*7)+(2*5)+(1*5)=150
150 % 10 = 0
So 92367-55-0 is a valid CAS Registry Number.

92367-55-0Relevant articles and documents

Radical Chain Reduction via Carbon Dioxide Radical Anion (CO2?-)

Hendy, Cecilia M.,Smith, Gavin C.,Xu, Zihao,Lian, Tianquan,Jui, Nathan T.

supporting information, p. 8987 - 8992 (2021/07/01)

We developed an effective method for reductive radical formation that utilizes the radical anion of carbon dioxide (CO2?-) as a powerful single electron reductant. Through a polarity matched hydrogen atom transfer (HAT) between an electrophilic radical and a formate salt, CO2?- formation occurs as a key element in a new radical chain reaction. Here, radical chain initiation can be performed through photochemical or thermal means, and we illustrate the ability of this approach to accomplish reductive activation of a range of substrate classes. Specifically, we employed this strategy in the intermolecular hydroarylation of unactivated alkenes with (hetero)aryl chlorides/bromides, radical deamination of arylammonium salts, aliphatic ketyl radical formation, and sulfonamide cleavage. We show that the reactivity of CO2?- with electron-poor olefins results in either single electron reduction or alkene hydrocarboxylation, where substrate reduction potentials can be utilized to predict reaction outcome.

PHENETANOLAMINE DERIVATIVES

-

Page/Page column 51, (2010/02/11)

Compounds of formula (I) and salts, solvates, and physiologically functional derivatives thereof, useful for the prophylaxis or treatment of a clinical condition for which a selective β2-adrenoreceptor agonist is indicated, for example asthma or chronic o

Oxabispidine compounds useful in the treatment of cardiac arrhyythmias

-

, (2008/06/13)

There is provided compounds of formula I, wherein R1, R2, R3, R4, R41to R46, A, B and G have meanings given in the description, which are useful in the prophylaxis and in the treatment of arrhythmias, in particular atrial and ventricular arrhythmias.

Potent in vitro and in vivo inhibitors of platelet aggregation based upon the Arg-Gly-Asp-Phe sequence of fibrinogen. A proposal on the nature of the binding interaction between the Arg-guanidine of RGDX mimetics and the platelet GP IIb-IIIa receptor

Zablocki,Miyano,Garland,Pireh,Schretzman,Rao,Lindmark,Panzer-Knodle,Nicholson,Taite,Salyers,King,Campion,Feigen

, p. 1811 - 1819 (2007/10/02)

Peptide mimetics of the RGDF sequence in which Arg-Gly has been replaced with 5-(4-amidinophenyl)pentanoyl mimetic has led to a 1000-fold increase in inhibitory potency over the natural RGDF ligand. The guanidine residue of the arginine may be involved in

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 92367-55-0