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146467-04-1

1-benzyl-3S-benzyloxy-4R-[1'R,2'S-O-isopropylidene-3'R,4'-dihydroxy]butyl 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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  • 146467-04-1 Structure

  • Basic information

    1. Product Name: 1-benzyl-3S-benzyloxy-4R-[1'R,2'S-O-isopropylidene-3'R,4'-dihydroxy]butyl azetidin-2-one
    2. Synonyms: 1-benzyl-3S-benzyloxy-4R-[1'R,2'S-O-isopropylidene-3'R,4'-dihydroxy]butyl azetidin-2-one
    3. CAS NO:146467-04-1
    4. Molecular Formula:
    5. Molecular Weight: 427.497
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 146467-04-1.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: 1-benzyl-3S-benzyloxy-4R-[1'R,2'S-O-isopropylidene-3'R,4'-dihydroxy]butyl azetidin-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-benzyl-3S-benzyloxy-4R-[1'R,2'S-O-isopropylidene-3'R,4'-dihydroxy]butyl azetidin-2-one(146467-04-1)
    11. EPA Substance Registry System: 1-benzyl-3S-benzyloxy-4R-[1'R,2'S-O-isopropylidene-3'R,4'-dihydroxy]butyl azetidin-2-one(146467-04-1)

  • 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: 146467-04-1(Hazardous Substances Data)

146467-04-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 146467-04-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,4,6 and 7 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 146467-04:
(8*1)+(7*4)+(6*6)+(5*4)+(4*6)+(3*7)+(2*0)+(1*4)=141
141 % 10 = 1
So 146467-04-1 is a valid CAS Registry Number.

146467-04-1Relevant articles and documents

Versatile β-Lactam Synthons: Enantiospecific Synthesis of (-)-Polyoxamic Acid

Banik, Bimal K.,Manhas, Maghar S.,Bose, Ajay K.

, p. 307 - 309 (1993)

An optically pure cis-α-hydroxy β-lactam of predictable absolute configuration prepared from readily available D-mannitol has been utilized for the synthesis of the non-natural enantiomer of polyoxamic acid through a series of stereospecific reactions.

Polyhydroxy amino acid derivatives via β-lactams using enantiospecific approaches and microwave techniques

Bose, Ajay K.,Banik, Bimal K.,Mathur, Chandra,Wagle, Dilip R.,Manhas, Maghar S.

, p. 5603 - 5619 (2007/10/03)

Enantiospecific synthesis has been developed for α-hydroxy β-lactams of predictable absolute configuration starting with readily available carbohydrates. Stereospecific approaches and microwave assisted chemical reactions have been utilized for the prepar

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