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CAS

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101067-86-1

(3R,4S)-3-Hydroxy-4-(4-methoxy-phenyl)-1,3-diphenyl-azetidin-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 101067-86-1 Structure

  • Basic information

    1. Product Name: (3R,4S)-3-Hydroxy-4-(4-methoxy-phenyl)-1,3-diphenyl-azetidin-2-one
    2. Synonyms: (3R,4S)-3-Hydroxy-4-(4-methoxy-phenyl)-1,3-diphenyl-azetidin-2-one
    3. CAS NO:101067-86-1
    4. Molecular Formula:
    5. Molecular Weight: 345.398
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 101067-86-1.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: (3R,4S)-3-Hydroxy-4-(4-methoxy-phenyl)-1,3-diphenyl-azetidin-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (3R,4S)-3-Hydroxy-4-(4-methoxy-phenyl)-1,3-diphenyl-azetidin-2-one(101067-86-1)
    11. EPA Substance Registry System: (3R,4S)-3-Hydroxy-4-(4-methoxy-phenyl)-1,3-diphenyl-azetidin-2-one(101067-86-1)

  • 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: 101067-86-1(Hazardous Substances Data)

101067-86-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 101067-86-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,0,6 and 7 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 101067-86:
(8*1)+(7*0)+(6*1)+(5*0)+(4*6)+(3*7)+(2*8)+(1*6)=81
81 % 10 = 1
So 101067-86-1 is a valid CAS Registry Number.

101067-86-1Downstream Products

101067-86-1Relevant articles and documents

STEREOSELECTIVE ANNELATION OF TRIMETHYLSILOXYACETIC ACIDS AND IMINES INTO 3-HYDROXY-β-LACTAMS

Cossio, Fernando P.,Palomo, Claudio

, p. 4239 - 4242 (2007/10/02)

Stereoselective synthesis of variously substituted 3-hydroxy-β-lactams can be achieved by the annelation of Schiff bases with trimethylsiloxyacetic acids promoted by phenyl dichlorophosphate reagent.A potential synthesis of N-unsubstituted β-lactams is ma

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