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207127-03-5

(S)-2-Benzyl-3-[(E)-hydroxyimino]-2-methyl-butyric 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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  • 207127-03-5 Structure

  • Basic information

    1. Product Name: (S)-2-Benzyl-3-[(E)-hydroxyimino]-2-methyl-butyric acid methyl ester
    2. Synonyms: (S)-2-Benzyl-3-[(E)-hydroxyimino]-2-methyl-butyric acid methyl ester
    3. CAS NO:207127-03-5
    4. Molecular Formula:
    5. Molecular Weight: 235.283
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 207127-03-5.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: (S)-2-Benzyl-3-[(E)-hydroxyimino]-2-methyl-butyric acid methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-2-Benzyl-3-[(E)-hydroxyimino]-2-methyl-butyric acid methyl ester(207127-03-5)
    11. EPA Substance Registry System: (S)-2-Benzyl-3-[(E)-hydroxyimino]-2-methyl-butyric acid methyl ester(207127-03-5)

  • 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: 207127-03-5(Hazardous Substances Data)

207127-03-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 207127-03-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,7,1,2 and 7 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 207127-03:
(8*2)+(7*0)+(6*7)+(5*1)+(4*2)+(3*7)+(2*0)+(1*3)=95
95 % 10 = 5
So 207127-03-5 is a valid CAS Registry Number.

207127-03-5Upstream product

207127-03-5Downstream Products

207127-03-5Relevant articles and documents

Synthesis of protected, chiral α,α-disubstituted α-amino acids via a Beckmann rearrangement

Frutos, Rogelio P.,Spero, Denice M.

, p. 2475 - 2478 (1998)

The synthesis of chiral, nonracemic, fully protected α,α- disubstituted α-amino acids via the Beckmann rearrangement of tosylated oximes 1 is described. The desired amino acids were obtained in good yields with excellent enantioselectivities in relatively few steps.

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