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(2R,3S)-2-Hydroxy-5-methyl-3-(toluene-4-sulfonylamino)-hexanoic acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • (2R,3S)-2-Hydroxy-5-methyl-3-(toluene-4-sulfonylamino)-hexanoic acid methyl ester

    Cas No: 201798-53-0

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  • 201798-53-0 Structure
  • Basic information

    1. Product Name: (2R,3S)-2-Hydroxy-5-methyl-3-(toluene-4-sulfonylamino)-hexanoic acid methyl ester
    2. Synonyms: (2R,3S)-2-Hydroxy-5-methyl-3-(toluene-4-sulfonylamino)-hexanoic acid methyl ester
    3. CAS NO:201798-53-0
    4. Molecular Formula:
    5. Molecular Weight: 329.417
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 201798-53-0.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: (2R,3S)-2-Hydroxy-5-methyl-3-(toluene-4-sulfonylamino)-hexanoic acid methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2R,3S)-2-Hydroxy-5-methyl-3-(toluene-4-sulfonylamino)-hexanoic acid methyl ester(201798-53-0)
    11. EPA Substance Registry System: (2R,3S)-2-Hydroxy-5-methyl-3-(toluene-4-sulfonylamino)-hexanoic acid methyl ester(201798-53-0)
  • 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: 201798-53-0(Hazardous Substances Data)

201798-53-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 201798-53-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,1,7,9 and 8 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 201798-53:
(8*2)+(7*0)+(6*1)+(5*7)+(4*9)+(3*8)+(2*5)+(1*3)=130
130 % 10 = 0
So 201798-53-0 is a valid CAS Registry Number.

201798-53-0Relevant articles and documents

Enantiospecific and diastereoselective synthesis of syn-β-amino-α-hydroxy acids

Sugimura, Hideyuki,Miura, Masayuki,Yamada, Nobuko

, p. 4089 - 4099 (2007/10/03)

The reaction of chiral α-hydroxy β,γ-unsaturated esters with tosyl isocyanate followed by cyclization of the resulting allylic carbamates with iodine in the presence of sodium carbonate provided trans-4,5-disubstituted 2-oxazolidinone derivatives in a highly diastereoselective manner. The subsequent removal of the iodo group and the protective functionality afforded the syn-β-amino-α-hydroxy acids. Using the reaction sequence, (2R,3S)- and (2S,3R)-3-amino-2-hydroxy acids were synthesized with high enantioselectivity.

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