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CAS

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76233-34-6

Butyl-(2,3-diphenyl-propyl)-methyl-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 76233-34-6 Structure

  • Basic information

    1. Product Name: Butyl-(2,3-diphenyl-propyl)-methyl-amine
    2. Synonyms:
    3. CAS NO:76233-34-6
    4. Molecular Formula:
    5. Molecular Weight: 281.441
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 76233-34-6.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: Butyl-(2,3-diphenyl-propyl)-methyl-amine(CAS DataBase Reference)
    10. NIST Chemistry Reference: Butyl-(2,3-diphenyl-propyl)-methyl-amine(76233-34-6)
    11. EPA Substance Registry System: Butyl-(2,3-diphenyl-propyl)-methyl-amine(76233-34-6)

  • 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: 76233-34-6(Hazardous Substances Data)

76233-34-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76233-34-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,2,3 and 3 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 76233-34:
(7*7)+(6*6)+(5*2)+(4*3)+(3*3)+(2*3)+(1*4)=126
126 % 10 = 6
So 76233-34-6 is a valid CAS Registry Number.

76233-34-6Downstream Products

76233-34-6Relevant articles and documents

Photochemical Addition of Tertiary Amines to Stilbene. Stereoelectronic Control of Tertiary Amine Oxidation.

Lewis, Frederick D.,Ho, Tong-Ing,Simpson, J. Thomas

, p. 1077 - 1082 (2007/10/02)

The photochemical addition reactions of seven nonsymmetrical tertiary amines with singlet trans-stilbene are described.Addition of methyldiisopropylamine or isopropyldimethylamine is highly selective for formation of the least substituted α-amino radical, whereas addition of several less highly branched amines is relatively nonselective.The product isotope effect for tert-butylmethyl(trideuteriomethyl)amine is 2.2+/-0.2.Product selectivity is determined by the orientation of the deprotonation of an aminium radical intermediate by the stilbene radical anion.Selectiveoxidation results from e stereoelectronic effect which is most evident w hen one more alkyl group is highly branched.

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