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50635-26-2

[4-(benzyloxy)phenoxy]acetonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 50635-26-2 Structure

  • Basic information

    1. Product Name: [4-(benzyloxy)phenoxy]acetonitrile
    2. Synonyms: [4-(benzyloxy)phenoxy]acetonitrile;2-[4-(benzyloxy)phenoxy]acetonitrile
    3. CAS NO:50635-26-2
    4. Molecular Formula: C15H13NO2
    5. Molecular Weight: 239.26922
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 50635-26-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: [4-(benzyloxy)phenoxy]acetonitrile(CAS DataBase Reference)
    10. NIST Chemistry Reference: [4-(benzyloxy)phenoxy]acetonitrile(50635-26-2)
    11. EPA Substance Registry System: [4-(benzyloxy)phenoxy]acetonitrile(50635-26-2)

  • 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: 50635-26-2(Hazardous Substances Data)

50635-26-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 50635-26-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,6,3 and 5 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 50635-26:
(7*5)+(6*0)+(5*6)+(4*3)+(3*5)+(2*2)+(1*6)=102
102 % 10 = 2
So 50635-26-2 is a valid CAS Registry Number.

50635-26-2Relevant articles and documents

Chloride-Anion-Templated Synthesis of a Strapped-Porphyrin-Containing Catenane Host System

Brown, Asha,Langton, Matthew J.,Kilah, Nathan L.,Thompson, Amber L.,Beer, Paul D.

supporting information, p. 17664 - 17675 (2015/12/08)

The synthesis, structure and anion-recognition properties of a new strapped-porphyrin-containing [2]catenane anion host system are described. The assembly of the catenane is directed by discrete chloride anion templation acting in synergy with secondary aromatic donor-acceptor and coordinative pyridine-zinc interactions. The [2]catenane incorporates a three-dimensional, hydrogen-bond-donating anion-binding pocket; solid-state structural analysis of the catenane-chloride complex reveals that the chloride anion is encapsulated within the catenane's interlocked binding cavity through six convergent CH...Cl and NH...Cl hydrogen-bonding interactions and solution-phase 1H NMR titration experiments demonstrate that this complementary hydrogen-bonding arrangement facilitates the selective recognition of chloride over larger halide anions in DMSO solution.

PTERIDINES AND THEIR USE AS AGROCHEMICALS

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Page/Page column 23, (2011/04/14)

The present disclosure relates to 1- or 2-(4-(aryloxy)-phenyl)ethylamino-, oxy- or sulfanyl)pteridines and 1- or 2-(4-(heteroaryloxy)-phenyl)ethylamino-, oxy- or sulfanyl)pteridines and their use as agrochemicals and animal health products.

PTERIDINES AND THEIR USE AS AGROCHEMICALS

-

Page/Page column 53, (2011/04/14)

The present disclosure relates to 1- or 2-(4-(aryloxy)-phenyl)ethylamino-, oxy- or sulfanyl)pteridines and 1- or 2-(4-(heteroaryloxy)-phenyl)ethylamino-, oxy- or sulfanyl)pteridines and their use as agrochemicals and animal health products.

The use of the cyanomethyl unit as a protecting group for phenols, amines and carbamates

Benarab,Boye,Savelon,Guillaumet

, p. 7567 - 7568 (2007/10/02)

The use of the cyanomethyl unit as a protecting group for phenols, primary and secondary amines, and carbamates is described. Optimized conditions for formation and hydrolysis of cyanomethyl in the presence of the other hydrogenolysis-sensitive groups such as O- and N-benzyl groups are presented.

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