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CAS

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143159-99-3

(3R,4S)-3-Benzyloxy-4-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-1-phenyl-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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  • 143159-99-3 Structure

  • Basic information

    1. Product Name: (3R,4S)-3-Benzyloxy-4-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-1-phenyl-azetidin-2-one
    2. Synonyms: (3R,4S)-3-Benzyloxy-4-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-1-phenyl-azetidin-2-one
    3. CAS NO:143159-99-3
    4. Molecular Formula:
    5. Molecular Weight: 353.418
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 143159-99-3.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: (3R,4S)-3-Benzyloxy-4-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-1-phenyl-azetidin-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (3R,4S)-3-Benzyloxy-4-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-1-phenyl-azetidin-2-one(143159-99-3)
    11. EPA Substance Registry System: (3R,4S)-3-Benzyloxy-4-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-1-phenyl-azetidin-2-one(143159-99-3)

  • 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: 143159-99-3(Hazardous Substances Data)

143159-99-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 143159-99-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,1,5 and 9 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 143159-99:
(8*1)+(7*4)+(6*3)+(5*1)+(4*5)+(3*9)+(2*9)+(1*9)=133
133 % 10 = 3
So 143159-99-3 is a valid CAS Registry Number.

143159-99-3Relevant articles and documents

Stereospecific novel glycosylation of hydroxy β-lactams via iodine-catalyzed reaction: A new method for optical resolution

Banik, Bimal K.,Manhas, Maghar S.

, p. 10769 - 10779 (2013/01/15)

Glycosylation of racemic and optically active α-hydroxy β-lactams by reaction with a few glycal derivatives in the presence of catalytic amounts of iodine has provided stereospecific formation of α-glycosides. This method has been extended for the prepara

MICROWAVE-INDUCED ORGANIC REACTION ENHANCEMENT CHEMISTRY. 4 CONVENIENT SYNTHESIS OF ENANTIOPURE α-HYDROXY-β-LACTAMS

Banik, Bimal K.,Manhas, Maghar S.,Kaluza, Zbignew,Barakat, Khaled J.,Bose, Ajay K.

, p. 3603 - 3606 (2007/10/02)

A convenient and rapid synthesis of enantiopure α-hydroxy-β-lactams using microwave-induced organic reaction enhancement chemistry has been developed.Reactions in domestic microwave ovens, which are very convenient and economical for small scale work in research or teaching laboratories, can also be conducted on a preparative scale of 100 - 500 g in simple beakers or flasks. Key Words: α-Hydroxy-β-lactams, microwave-induced organic reactions, enantiospecific synthesis

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