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CAS

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146877-28-3

(S)-4-(benzyloxy)-1-phenylbutan-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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  • 146877-28-3 Structure

  • Basic information

    1. Product Name: (S)-4-(benzyloxy)-1-phenylbutan-2-ol
    2. Synonyms: (S)-4-(benzyloxy)-1-phenylbutan-2-ol
    3. CAS NO:146877-28-3
    4. Molecular Formula:
    5. Molecular Weight: 256.345
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 146877-28-3.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: (S)-4-(benzyloxy)-1-phenylbutan-2-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-4-(benzyloxy)-1-phenylbutan-2-ol(146877-28-3)
    11. EPA Substance Registry System: (S)-4-(benzyloxy)-1-phenylbutan-2-ol(146877-28-3)

  • 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: 146877-28-3(Hazardous Substances Data)

146877-28-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 146877-28-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,8,7 and 7 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 146877-28:
(8*1)+(7*4)+(6*6)+(5*8)+(4*7)+(3*7)+(2*2)+(1*8)=173
173 % 10 = 3
So 146877-28-3 is a valid CAS Registry Number.

146877-28-3Relevant articles and documents

Stereocontrolled Total Synthesis of 9(R)-N-BOC-Ahda Methyl Ester

Chakraborty, Tushar K,Hussain, Azhar K,Joshi, Subodh P

, p. 2385 - 2388 (1992)

An efficient convergent route to the first total synthesis of 9(R)-N-BOC-Ahda methyl ester, in optically pure form, is described.

Carbohydrate-Catalyzed Enantioselective Alkene Diboration: Enhanced Reactivity of 1,2-Bonded Diboron Complexes

Fang, Lichao,Yan, Lu,Haeffner, Fredrik,Morken, James P.

supporting information, p. 2508 - 2511 (2016/03/12)

Catalytic enantioselective diboration of alkenes is accomplished with readily available carbohydrate-derived catalysts. Mechanistic experiments suggest the intermediacy of 1,2-bonded diboronates.

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