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71491-50-4

(R)-2,3-dimethyl-3-phenyl-pentan-2-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 71491-50-4 Structure

  • Basic information

    1. Product Name: (R)-2,3-dimethyl-3-phenyl-pentan-2-ol
    2. Synonyms: (R)-2,3-dimethyl-3-phenyl-pentan-2-ol
    3. CAS NO:71491-50-4
    4. Molecular Formula:
    5. Molecular Weight: 192.301
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 71491-50-4.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: (R)-2,3-dimethyl-3-phenyl-pentan-2-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-2,3-dimethyl-3-phenyl-pentan-2-ol(71491-50-4)
    11. EPA Substance Registry System: (R)-2,3-dimethyl-3-phenyl-pentan-2-ol(71491-50-4)

  • 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: 71491-50-4(Hazardous Substances Data)

71491-50-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71491-50-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,4,9 and 1 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 71491-50:
(7*7)+(6*1)+(5*4)+(4*9)+(3*1)+(2*5)+(1*0)=124
124 % 10 = 4
So 71491-50-4 is a valid CAS Registry Number.

71491-50-4Relevant articles and documents

PHOTOCHEMICAL OXIDATION AND DIMERIZATION OF ALKYLBENZENES. SELECTIVE REACTIONS OF THE ALKYL SIDE GROUPS

Pasternak, Mordechai,Morduchowitz, Abraham

, p. 4275 - 4278 (2007/10/02)

Irradiations of alkylbenzene compounds in an oxygen atmosphere result exclusively in oxidation reactions, while in a less oxidative environment dimerization processes predominate.Under all conditions studied, the reactions took place only at one benzyl position.

PHOTOSUBSTITUTION OF BENZYL HYDROGENS WITH ALCOHOLIC MOIETIES. SELECTIVE FORMATION OF ALKYLBENZENE CARBINOLS

Pasternak, Mordechai,Morduchowitz, Abraham

, p. 3439 - 3442 (2007/10/02)

Irradiations of alkylbenzene compounds with various alcohols in an air atmosphere, resulted in substitution of the benzyl hydrogens with alcoholic moieties in a very selective mode.

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