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CAS

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133038-96-7

[(2S,3S)-3-(Trityl-amino)-tetrahydro-furan-2-yl]-acetic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 133038-96-7 Structure

  • Basic information

    1. Product Name: [(2S,3S)-3-(Trityl-amino)-tetrahydro-furan-2-yl]-acetic acid
    2. Synonyms:
    3. CAS NO:133038-96-7
    4. Molecular Formula:
    5. Molecular Weight: 387.478
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 133038-96-7.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: [(2S,3S)-3-(Trityl-amino)-tetrahydro-furan-2-yl]-acetic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: [(2S,3S)-3-(Trityl-amino)-tetrahydro-furan-2-yl]-acetic acid(133038-96-7)
    11. EPA Substance Registry System: [(2S,3S)-3-(Trityl-amino)-tetrahydro-furan-2-yl]-acetic acid(133038-96-7)

  • 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: 133038-96-7(Hazardous Substances Data)

133038-96-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 133038-96-7 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 6 respectively.
Calculate Digit Verification of CAS Registry Number 133038-96:
(8*1)+(7*3)+(6*3)+(5*0)+(4*3)+(3*8)+(2*9)+(1*6)=107
107 % 10 = 7
So 133038-96-7 is a valid CAS Registry Number.

133038-96-7Downstream Products

133038-96-7Relevant articles and documents

Total syntheses of novel dideoxynucleoside analogues using chiral amino acids

Balayiannis,Karigiannis,Gatos,Papaioannou,De Clercq

, p. 6191 - 6194 (2007/10/03)

N-Tritylated L- and D-methionine and L-glutamic acid were used to obtain novel chiral iso-dideoxynucleoside analogues incorporating a tetrahydrofuranyl or a tetrahyropyranyl ring as the pseudosugar part, and at positions 2 and 3 of the ring an hydroxyethyl group and thymine or adenine, respectively. (C) 2000 Elsevier Science Ltd.

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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