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129508-05-0

(4S,5S)-5-Hydroxy-4-[hydroxy-((R)-1-phenyl-ethyl)-amino]-tetrahydro-pyran-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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  • 129508-05-0 Structure

  • Basic information

    1. Product Name: (4S,5S)-5-Hydroxy-4-[hydroxy-((R)-1-phenyl-ethyl)-amino]-tetrahydro-pyran-2-one
    2. Synonyms:
    3. CAS NO:129508-05-0
    4. Molecular Formula:
    5. Molecular Weight: 251.282
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 129508-05-0.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: (4S,5S)-5-Hydroxy-4-[hydroxy-((R)-1-phenyl-ethyl)-amino]-tetrahydro-pyran-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (4S,5S)-5-Hydroxy-4-[hydroxy-((R)-1-phenyl-ethyl)-amino]-tetrahydro-pyran-2-one(129508-05-0)
    11. EPA Substance Registry System: (4S,5S)-5-Hydroxy-4-[hydroxy-((R)-1-phenyl-ethyl)-amino]-tetrahydro-pyran-2-one(129508-05-0)

  • 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: 129508-05-0(Hazardous Substances Data)

129508-05-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 129508-05-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,5,0 and 8 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 129508-05:
(8*1)+(7*2)+(6*9)+(5*5)+(4*0)+(3*8)+(2*0)+(1*5)=130
130 % 10 = 0
So 129508-05-0 is a valid CAS Registry Number.

129508-05-0Downstream Products

129508-05-0Relevant articles and documents

SYNTHESIS OF A POTENTIAL INTERMEDIATE TO β-LACTAM ANTIBIOTICS

Freer, Andrew,Overton, Karl,Tomanek, Richard

, p. 1471 - 1474 (2007/10/02)

Cycloaddition of nitrone (2) to α-chloroacrylonitrile followed by hydrolysis afforded the isoxazolidinone (1) as a single diastereomer.The configuration at the new chiral centre (3S), corresponding to that in thienamycin, was established by an X-ray analy

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