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Methyl-((S)-2-phenyl-1-thiocarbamoyl-ethyl)-carbamic acid benzyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 386743-17-5 Structure
  • Basic information

    1. Product Name: Methyl-((S)-2-phenyl-1-thiocarbamoyl-ethyl)-carbamic acid benzyl ester
    2. Synonyms: Methyl-((S)-2-phenyl-1-thiocarbamoyl-ethyl)-carbamic acid benzyl ester
    3. CAS NO:386743-17-5
    4. Molecular Formula:
    5. Molecular Weight: 328.435
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 386743-17-5.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-((S)-2-phenyl-1-thiocarbamoyl-ethyl)-carbamic acid benzyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Methyl-((S)-2-phenyl-1-thiocarbamoyl-ethyl)-carbamic acid benzyl ester(386743-17-5)
    11. EPA Substance Registry System: Methyl-((S)-2-phenyl-1-thiocarbamoyl-ethyl)-carbamic acid benzyl ester(386743-17-5)
  • 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: 386743-17-5(Hazardous Substances Data)

386743-17-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 386743-17-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,6,7,4 and 3 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 386743-17:
(8*3)+(7*8)+(6*6)+(5*7)+(4*4)+(3*3)+(2*1)+(1*7)=185
185 % 10 = 5
So 386743-17-5 is a valid CAS Registry Number.

386743-17-5Relevant articles and documents

Synthesis of the marine natural product barbamide

Nguyen,Willis,Gerwick

, p. 1934 - 1935 (2001)

The first total synthesis of the trichlorinated natural product barbamide is described. The convergent approach involves coupling (S)-3-trichloromethylbutanoyl chloride with Meldrum's acid (2,2-dimethyl-1,3-dioxane-4,6-dione) to give 15 followed by additi

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