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221205-18-1

[(R)-1-(2-Hydroxy-ethyl)-3-methylsulfanyl-propyl]-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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  • 221205-18-1 Structure

  • Basic information

    1. Product Name: [(R)-1-(2-Hydroxy-ethyl)-3-methylsulfanyl-propyl]-carbamic acid benzyl ester
    2. Synonyms:
    3. CAS NO:221205-18-1
    4. Molecular Formula:
    5. Molecular Weight: 283.392
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 221205-18-1.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: [(R)-1-(2-Hydroxy-ethyl)-3-methylsulfanyl-propyl]-carbamic acid benzyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: [(R)-1-(2-Hydroxy-ethyl)-3-methylsulfanyl-propyl]-carbamic acid benzyl ester(221205-18-1)
    11. EPA Substance Registry System: [(R)-1-(2-Hydroxy-ethyl)-3-methylsulfanyl-propyl]-carbamic acid benzyl ester(221205-18-1)

  • 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: 221205-18-1(Hazardous Substances Data)

221205-18-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 221205-18-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,1,2,0 and 5 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 221205-18:
(8*2)+(7*2)+(6*1)+(5*2)+(4*0)+(3*5)+(2*1)+(1*8)=71
71 % 10 = 1
So 221205-18-1 is a valid CAS Registry Number.

221205-18-1Upstream product

221205-18-1Downstream Products

221205-18-1Relevant articles and documents

Convenient in situ synthesis of nonracemic N-protected β-amino aldehydes from β-amino acids. Applications in Wittig reactions and heterocycle synthesis

Davies, Simon B.,McKervey, M. Anthony

, p. 1229 - 1232 (1999)

N-Z-γ-amino alcohols derived from nonracemic β-amino acids are smoothly oxidised by manganese dioxide in acetonitrile to afford aldehydes which can be trapped in situ in Wittig reactions with carbonyl-substituted phosphoranes. The application of this methodology to the synthesis of the alkaloids (S)-(+)-N-BOC-coniine, (S)-(-)-coniceine and a pipecoline precursor is described.

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