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CAS

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160712-05-0

Acetic acid (S)-3-((R)-1-benzyl-5-oxo-pyrazolidin-3-yl)-2-hydroxy-propyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 160712-05-0 Structure

  • Basic information

    1. Product Name: Acetic acid (S)-3-((R)-1-benzyl-5-oxo-pyrazolidin-3-yl)-2-hydroxy-propyl ester
    2. Synonyms:
    3. CAS NO:160712-05-0
    4. Molecular Formula:
    5. Molecular Weight: 292.335
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 160712-05-0.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: Acetic acid (S)-3-((R)-1-benzyl-5-oxo-pyrazolidin-3-yl)-2-hydroxy-propyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Acetic acid (S)-3-((R)-1-benzyl-5-oxo-pyrazolidin-3-yl)-2-hydroxy-propyl ester(160712-05-0)
    11. EPA Substance Registry System: Acetic acid (S)-3-((R)-1-benzyl-5-oxo-pyrazolidin-3-yl)-2-hydroxy-propyl ester(160712-05-0)

  • 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: 160712-05-0(Hazardous Substances Data)

160712-05-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 160712-05-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,7,1 and 2 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 160712-05:
(8*1)+(7*6)+(6*0)+(5*7)+(4*1)+(3*2)+(2*0)+(1*5)=100
100 % 10 = 0
So 160712-05-0 is a valid CAS Registry Number.

160712-05-0Relevant articles and documents

Addition of N-benzylhydrazine to sugar δ-enlactones

Panfil,Krajewski,Gluzinski,Stefaniak,Chmielewski

, p. 7219 - 7230 (2007/10/02)

The conjugate addition - rearrangement of N-benzylhydrazine to sugar δ- enlactone with erythro configuration 1 and 2 affords mixtures of respective ribo and arabino isomers with the former one prevailing. In the case of the threo lactone 3 two regioisomers with xylo configuration are produced, whereas in the case of 4 only one isomer with the erythro configuration is formed. The stereochemical course of these reactions was explained.

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