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CAS

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721926-04-1

(2-bromo-1,1-dideuteroprop-2-enyl)-[(S)-1-phenylethyl]amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 721926-04-1 Structure

  • Basic information

    1. Product Name: (2-bromo-1,1-dideuteroprop-2-enyl)-[(S)-1-phenylethyl]amine
    2. Synonyms: (2-bromo-1,1-dideuteroprop-2-enyl)-[(S)-1-phenylethyl]amine
    3. CAS NO:721926-04-1
    4. Molecular Formula:
    5. Molecular Weight: 242.127
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 721926-04-1.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: (2-bromo-1,1-dideuteroprop-2-enyl)-[(S)-1-phenylethyl]amine(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2-bromo-1,1-dideuteroprop-2-enyl)-[(S)-1-phenylethyl]amine(721926-04-1)
    11. EPA Substance Registry System: (2-bromo-1,1-dideuteroprop-2-enyl)-[(S)-1-phenylethyl]amine(721926-04-1)

  • 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: 721926-04-1(Hazardous Substances Data)

721926-04-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 721926-04-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,2,1,9,2 and 6 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 721926-04:
(8*7)+(7*2)+(6*1)+(5*9)+(4*2)+(3*6)+(2*0)+(1*4)=151
151 % 10 = 1
So 721926-04-1 is a valid CAS Registry Number.

721926-04-1Relevant articles and documents

Rare example of nucleophilic substitution at vinylic carbon with inversion: Mechanism of methyleneaziridine formation by sodium amide induced ring closure revisited

Shiers, Jason J.,Shipman, Michael,Hayes, Jerome F.,Slawin, Alexandra M. Z.

, p. 6868 - 6869 (2007/10/03)

Intramolecular nucleophilic substitution of the C-Br bond of (E)- and (Z)-2-bromobut-2-enylamines by the pendant nitrogen atom leads to 2-ethyleneaziridines by way of stereochemical inversion at the vinylic carbon atom. The stereochemistry of the products is unambiguously established by X-ray crystallography performed on two derivatives. These cyclizations represent some of the first examples of substitution with inversion in unactivated vinylic substrates. In conjunction with additional deuterium-labeling experiments, the accepted mechanism for this reaction is shown to be flawed. Copyright

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