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Benzenemethanamine, N-[(4-bromophenyl)methylene]-a-methyl-, (S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 67463-03-0 Structure
  • Basic information

    1. Product Name: Benzenemethanamine, N-[(4-bromophenyl)methylene]-a-methyl-, (S)-
    2. Synonyms:
    3. CAS NO:67463-03-0
    4. Molecular Formula: C15H14BrN
    5. Molecular Weight: 288.187
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 67463-03-0.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: Benzenemethanamine, N-[(4-bromophenyl)methylene]-a-methyl-, (S)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzenemethanamine, N-[(4-bromophenyl)methylene]-a-methyl-, (S)-(67463-03-0)
    11. EPA Substance Registry System: Benzenemethanamine, N-[(4-bromophenyl)methylene]-a-methyl-, (S)-(67463-03-0)
  • 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: 67463-03-0(Hazardous Substances Data)

67463-03-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67463-03-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,4,6 and 3 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 67463-03:
(7*6)+(6*7)+(5*4)+(4*6)+(3*3)+(2*0)+(1*3)=140
140 % 10 = 0
So 67463-03-0 is a valid CAS Registry Number.

67463-03-0Relevant articles and documents

Carbamoyl anion addition to nitrones

Reeves, Jonathan T.,Lorenc, Chris,Camara, Kaddy,Li, Zhibin,Lee, Heewon,Busacca, Carl A.,Senanayake, Chris H.

, p. 5895 - 5902 (2014)

The addition of carbamoyl anions derived from N,N-disubstituted formamides and LDA to N-tert-butyl nitrones is described. The reaction was demonstrated with a variety of formamides and nitrones and provided a direct route to α-(N-hydroxy)amino amides. The use of a tert-leucinol derived chiral auxiliary on the nitrone provided products in good diastereoselectivity. Derivatization of the products by tert-butyl deprotection or N-deoxygenation was demonstrated.

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