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485831-41-2

Carbamic acid, [(3S)-3-[[(1,1-dimethylethoxy)carbonyl]amino]-2-oxo-1-azetidinyl]methyl- , phenylmethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 485831-41-2 Structure

  • Basic information

    1. Product Name: Carbamic acid, [(3S)-3-[[(1,1-dimethylethoxy)carbonyl]amino]-2-oxo-1-azetidinyl]methyl- , phenylmethyl ester
    2. Synonyms:
    3. CAS NO:485831-41-2
    4. Molecular Formula: C17H23N3O5
    5. Molecular Weight: 349.387
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 485831-41-2.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: Carbamic acid, [(3S)-3-[[(1,1-dimethylethoxy)carbonyl]amino]-2-oxo-1-azetidinyl]methyl- , phenylmethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Carbamic acid, [(3S)-3-[[(1,1-dimethylethoxy)carbonyl]amino]-2-oxo-1-azetidinyl]methyl- , phenylmethyl ester(485831-41-2)
    11. EPA Substance Registry System: Carbamic acid, [(3S)-3-[[(1,1-dimethylethoxy)carbonyl]amino]-2-oxo-1-azetidinyl]methyl- , phenylmethyl ester(485831-41-2)

  • 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: 485831-41-2(Hazardous Substances Data)

485831-41-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 485831-41-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,8,5,8,3 and 1 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 485831-41:
(8*4)+(7*8)+(6*5)+(5*8)+(4*3)+(3*1)+(2*4)+(1*1)=182
182 % 10 = 2
So 485831-41-2 is a valid CAS Registry Number.

485831-41-2Relevant articles and documents

The synthesis of azapeptidomimetic beta-lactam molecules as potential protease inhibitors.

Malachowski, William P,Tie, Chenyang,Wang, Katherine,Broadrup, Robert L

, p. 8962 - 8969 (2007/10/03)

Synthetic methods for the construction of a novel peptidomimetic structure are reported. The structure incorporates a beta-lactam and an azapeptide in a peptide backbone with the intention of generating rationally designed substrate-based protease inhibitors. The beta-lactam is formed by subjecting serine or threonine-azapeptides to Mitsunobu reaction conditions. Importantly, the azapeptidomimetic beta-lactam structure permits extended binding inhibition and the synthetic methods to create tetrapeptidomimetic structures are described.

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