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101067-93-0

Benzoic acid (R)-1-((2R,3S)-2-ethoxycarbonylmethyl-4-oxo-azetidin-3-yl)-ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 101067-93-0 Structure

  • Basic information

    1. Product Name: Benzoic acid (R)-1-((2R,3S)-2-ethoxycarbonylmethyl-4-oxo-azetidin-3-yl)-ethyl ester
    2. Synonyms:
    3. CAS NO:101067-93-0
    4. Molecular Formula:
    5. Molecular Weight: 305.331
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 101067-93-0.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: Benzoic acid (R)-1-((2R,3S)-2-ethoxycarbonylmethyl-4-oxo-azetidin-3-yl)-ethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzoic acid (R)-1-((2R,3S)-2-ethoxycarbonylmethyl-4-oxo-azetidin-3-yl)-ethyl ester(101067-93-0)
    11. EPA Substance Registry System: Benzoic acid (R)-1-((2R,3S)-2-ethoxycarbonylmethyl-4-oxo-azetidin-3-yl)-ethyl ester(101067-93-0)

  • 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: 101067-93-0(Hazardous Substances Data)

101067-93-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 101067-93-0 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, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 101067-93:
(8*1)+(7*0)+(6*1)+(5*0)+(4*6)+(3*7)+(2*9)+(1*3)=80
80 % 10 = 0
So 101067-93-0 is a valid CAS Registry Number.

101067-93-0Downstream Products

101067-93-0Relevant articles and documents

A FACILE, STEREOCONTROLLED ENTRY TO KEY INTERMEDIATES FOR THIENAMYCIN SYNTHESIS FROM ETHYL (S)-3-HYDROXYBUTANOATE

Chiba, Toshiyuki,Nagatsuma, Masako,Nakai, Takeshi

, p. 1343 - 1346 (2007/10/02)

A new synthetic approach to optically active key intermediates for thienamycin synthesis is described which involves the highly stereocontrolled transformation of the 2-azetidinone obtained via the condensation of ethyl (S)-3-hydroxybutanoate with the N-s

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