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133038-99-0

methyl (4R)-6-hydroxy-4-(tritylamino)hexanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 133038-99-0 Structure

  • Basic information

    1. Product Name: methyl (4R)-6-hydroxy-4-(tritylamino)hexanoate
    2. Synonyms:
    3. CAS NO:133038-99-0
    4. Molecular Formula:
    5. Molecular Weight: 403.521
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 133038-99-0.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: methyl (4R)-6-hydroxy-4-(tritylamino)hexanoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl (4R)-6-hydroxy-4-(tritylamino)hexanoate(133038-99-0)
    11. EPA Substance Registry System: methyl (4R)-6-hydroxy-4-(tritylamino)hexanoate(133038-99-0)

  • 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: 133038-99-0(Hazardous Substances Data)

133038-99-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 133038-99-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,0,3 and 8 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 133038-99:
(8*1)+(7*3)+(6*3)+(5*0)+(4*3)+(3*8)+(2*9)+(1*9)=110
110 % 10 = 0
So 133038-99-0 is a valid CAS Registry Number.

133038-99-0Downstream Products

133038-99-0Relevant articles and documents

Synthesis of Conformationally Restricted Chiral γ-Aminobutyric Acid (GABA) Analogues

Papaioannou, Dionissios,Stavropoulos, George,Sivas, Manolis,Barlos, Kleomenis,Francis, George W.,et al.

, p. 99 - 104 (2007/10/02)

The epimeric (2S, 3S)- and (2R, 3S)-3-amino-2-(carboxymethyl)oxolanes have been synthesised from (S)-N-tritylhomoserine lactone.The lactone was first reduced with diisobutylaluminium hydride to a diastereomeric mixture of the corresponding lactols which u

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