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67213-45-0

2-phenylethanol-1,2-d2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 67213-45-0 Structure

  • Basic information

    1. Product Name: 2-phenylethanol-1,2-d2
    2. Synonyms: 2-phenylethanol-1,2-d2
    3. CAS NO:67213-45-0
    4. Molecular Formula:
    5. Molecular Weight: 124.151
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 67213-45-0.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: 2-phenylethanol-1,2-d2(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-phenylethanol-1,2-d2(67213-45-0)
    11. EPA Substance Registry System: 2-phenylethanol-1,2-d2(67213-45-0)

  • 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: 67213-45-0(Hazardous Substances Data)

67213-45-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67213-45-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,2,1 and 3 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 67213-45:
(7*6)+(6*7)+(5*2)+(4*1)+(3*3)+(2*4)+(1*5)=120
120 % 10 = 0
So 67213-45-0 is a valid CAS Registry Number.

67213-45-0Relevant articles and documents

CATALYTIC ANTI-MARKOVNIKOV OXIDATION AND HYDRATION OF OLEFINS

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Page/Page column 18, (2012/07/14)

The disclosure provides a dual-catalysis system for direct conversion of olefins to alcohols. The cooperative catalytic system contains one oxidizing catalyst and one transfer-hydrogenation catalyst. A wide variety of olefins, including aromatic and aliphatic olefins, can be used as the reactant. The transformation proceeds with anti-Markovnikov selectivity, and in some aspects provides primary alcohols as major products. The disclosure further provides a system for oxidation of olefins with anti-Markovnikov selectivity.

Mechanism of elimination rections. 40. Attempted study of stereochemistry of elimination from 2-(p-nitrophenyl)ethyltrimmethylammonium ion. Base-promoted cis-trans isomerization of p-nitrostyrene-β-d1

Dohner, Brent R.,Saunders, William H., Jr.

, p. 1026 - 1030 (2007/10/02)

Stereospecifically deuterated ArCHDCHDNMe3+I- and ArCHDCHDNMe2O have been prepared, where Ar=C6H5 and p-NO2C6H4.When Ar=C6H5, the elimination reaction of the quaternery salt with ethoxide in ethanol goes with >98percent anti stereoch

Stereochemical Course of the "Mixed Hydride" (AlD3 and AlCl2H) Reduction of Optically Active Styrene-2,2-d2 Oxide

Elsenbaumer, R. L.,Mosher, Harry S.,Morrison, James D.,Tomaszewski, J. E.

, p. 4034 - 4038 (2007/10/02)

The reduction of (R)-(+)-styrene-2,2-d2 oxide with aluminum deuteride (AlD3) in diethyl ether at 0 deg C gives a nearly equal mixture of (S)-(+)-1-phenylethanol-2,2,2-d3 and (S)-(-)-2-phenylethanol-1,1,2-d3, the latter being formed with almost complete in

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