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[2-(4-Bromo-phenyl)-ethyl]-ethyl-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 132336-05-1 Structure
  • Basic information

    1. Product Name: [2-(4-Bromo-phenyl)-ethyl]-ethyl-amine
    2. Synonyms: [2-(4-Bromo-phenyl)-ethyl]-ethyl-amine
    3. CAS NO:132336-05-1
    4. Molecular Formula:
    5. Molecular Weight: 228.132
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 132336-05-1.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-(4-Bromo-phenyl)-ethyl]-ethyl-amine(CAS DataBase Reference)
    10. NIST Chemistry Reference: [2-(4-Bromo-phenyl)-ethyl]-ethyl-amine(132336-05-1)
    11. EPA Substance Registry System: [2-(4-Bromo-phenyl)-ethyl]-ethyl-amine(132336-05-1)
  • 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: 132336-05-1(Hazardous Substances Data)

132336-05-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132336-05-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,3,3 and 6 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 132336-05:
(8*1)+(7*3)+(6*2)+(5*3)+(4*3)+(3*6)+(2*0)+(1*5)=91
91 % 10 = 1
So 132336-05-1 is a valid CAS Registry Number.

132336-05-1Downstream Products

132336-05-1Relevant articles and documents

Direct Reductive N-Functionalization of Aliphatic Nitro Compounds

Rauser, Marian,Ascheberg, Christoph,Niggemann, Meike

, p. 3970 - 3974 (2018/02/26)

The first general protocol for the direct reductive N-functionalization of aliphatic nitro compounds is presented. The nitro group is partially reduced to a nitrenoid, with a mild and readily available combination of B2pin2 and zinc organyls. Thereby, the formation of an unstable nitroso intermediate is avoided, which has so far severely limited reductive transformations of aliphatic nitro compounds. The reaction is concluded by an electrophilic amination of zinc organyls.

Selected reductions of conjugated nitroalkenes

Kabalka, George W.,Laila Guindi,Varma, Rajender S.

, p. 7443 - 7457 (2007/10/02)

Conjugated nitroalkenes are readily reduced by a variety of borane and borohydride reagents. The reactions provide a convenient access to a number of nitrogen and oxygen based functional groups.

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