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(S)-5-(N-benzyloxycarbonyl-L-prolyloxy)-1-methylimidazolidine-2,4-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 121146-03-0 Structure
  • Basic information

    1. Product Name: (S)-5-(N-benzyloxycarbonyl-L-prolyloxy)-1-methylimidazolidine-2,4-dione
    2. Synonyms:
    3. CAS NO:121146-03-0
    4. Molecular Formula:
    5. Molecular Weight: 361.354
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 121146-03-0.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: (S)-5-(N-benzyloxycarbonyl-L-prolyloxy)-1-methylimidazolidine-2,4-dione(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-5-(N-benzyloxycarbonyl-L-prolyloxy)-1-methylimidazolidine-2,4-dione(121146-03-0)
    11. EPA Substance Registry System: (S)-5-(N-benzyloxycarbonyl-L-prolyloxy)-1-methylimidazolidine-2,4-dione(121146-03-0)
  • 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: 121146-03-0(Hazardous Substances Data)

121146-03-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 121146-03-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,1,4 and 6 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 121146-03:
(8*1)+(7*2)+(6*1)+(5*1)+(4*4)+(3*6)+(2*0)+(1*3)=70
70 % 10 = 0
So 121146-03-0 is a valid CAS Registry Number.

121146-03-0Downstream Products

121146-03-0Relevant articles and documents

The Stepwise Mammalian Oxidation of the Hydantoin 1-Methylimidazolidine-2,4-dione into Methylimidazolidinetrione via 5-Hydroxy-1-methyl-imidazolidine-2,4-dione

Ienaga, Kazuharu,Nakamura, Ko,Ishii, Akira,Taga, Tooru,Miwa, Yoshihisa,Yoneda, Fumio

, p. 1153 - 1156 (1989)

The metabolism of 1-methylhydantoin (2) is described.The major and general metabolic route in mammals, represented by formulae (2) to (7), includes two consecutive stepwise oxidations giving 5-hydroxy-1-methylhydantoin (3) and thence 1-methylparabanic acid (4).Since the first oxidation proved to be stereoselective, the step was thought to be enzymatic.Although enantiomeric products (3a) and (3b) (ca. 3:1) could not be separated directly, the mixture was converted into (S)- and (R)-5-(N-benzyloxycarbonyl-L-prolyloxy)-1-methylhydantoins (13a) and (13b) which proved separable and were identified by X-ray analysis of the (R)-diastereoisomer.The regioselective ring-fission of the second product (4) into the methyloxaluric acid (5) is discussed.Two minor oxidative routes from the substrate (2) into sarcosine (9) and parabanic acid (10) were also shown to exist.

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