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125593-33-1

2-ethoxymethyl-phenethyl alcohol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 125593-33-1 Structure

  • Basic information

    1. Product Name: 2-ethoxymethyl-phenethyl alcohol
    2. Synonyms: 2-ethoxymethyl-phenethyl alcohol
    3. CAS NO:125593-33-1
    4. Molecular Formula:
    5. Molecular Weight: 180.247
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 125593-33-1.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-ethoxymethyl-phenethyl alcohol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-ethoxymethyl-phenethyl alcohol(125593-33-1)
    11. EPA Substance Registry System: 2-ethoxymethyl-phenethyl alcohol(125593-33-1)

  • 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: 125593-33-1(Hazardous Substances Data)

125593-33-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 125593-33-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,5,9 and 3 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 125593-33:
(8*1)+(7*2)+(6*5)+(5*5)+(4*9)+(3*3)+(2*3)+(1*3)=131
131 % 10 = 1
So 125593-33-1 is a valid CAS Registry Number.

125593-33-1Relevant articles and documents

Carbenes and the O-H Bond: Hydroxyalkyl-Substituted Arylcarbenes

Kirmse, Wolfgang,Kund, Klaus

, p. 2325 - 2332 (2007/10/02)

carbene (4), phenylcarbene (19), and carbene (30) have been generated by photolysis of tosylhydrazone or diazo precursors in protic solvents.These carbenes give cyclic ethers (7, 18, 33) competitively with insertion into O-H bonds of the solvent.For comparison, the analogous benzyl cations (9, 17, 31) have been generated by solvolysis or dediazoniation.The cations are more sensitive to structural variation than their carbenic counterparts: 9 does not undergo intramolecular nucleophilic substitution, in contrast to 17 and 31.These observations are explicable in terms of high barriers for rotation about aryl-cation bonds, as compared with low barriers for rotation about aryl-carbene bonds.Two major effects of the solvent (ROH) and of the base (RONa) on product formation may be distinguished: (i) protonation of the carbene (or of its precursors) in the more acidic media leads to predominantly cationic processes; (ii) deprotonation of the OH group under strongly basic conditions enhances the nucleophilicity of the oxygen, and also facilitates insertion into the α-C-H bonds of 30.

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