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133038-76-3

(-)-(R)-methyl-2-(N,N'diisopropylcarbamoyloxy)-2-phenylpropanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • (-)-(R)-methyl-2-(N,N'diisopropylcarbamoyloxy)-2-phenylpropanoate

    Cas No: 133038-76-3

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  • 133038-76-3 Structure

  • Basic information

    1. Product Name: (-)-(R)-methyl-2-(N,N'diisopropylcarbamoyloxy)-2-phenylpropanoate
    2. Synonyms: (-)-(R)-methyl-2-(N,N'diisopropylcarbamoyloxy)-2-phenylpropanoate
    3. CAS NO:133038-76-3
    4. Molecular Formula:
    5. Molecular Weight: 307.39
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 133038-76-3.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)-methyl-2-(N,N'diisopropylcarbamoyloxy)-2-phenylpropanoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (-)-(R)-methyl-2-(N,N'diisopropylcarbamoyloxy)-2-phenylpropanoate(133038-76-3)
    11. EPA Substance Registry System: (-)-(R)-methyl-2-(N,N'diisopropylcarbamoyloxy)-2-phenylpropanoate(133038-76-3)

  • 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: 133038-76-3(Hazardous Substances Data)

133038-76-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 133038-76-3 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, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 133038-76:
(8*1)+(7*3)+(6*3)+(5*0)+(4*3)+(3*8)+(2*7)+(1*6)=103
103 % 10 = 3
So 133038-76-3 is a valid CAS Registry Number.

133038-76-3Downstream Products

133038-76-3Relevant articles and documents

Generation of a configurationally stable, enantioenriched α-oxy-α-methylbenzyllithium: Stereodivergence of its electrophilic substitution

Carstens, Axel,Hoppe, Dieter

, p. 6097 - 6108 (2007/10/02)

The deprotonation of (R)- or (S)-1-phenylethyl N,N-diisopropylcarbamate with s-butyllithium/TMEDA in unpolar solvents (e.g. ether or hexane) at -78°C produces configurationally stable ion pairs which are substituted stereospecifically by different electro

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