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CAS

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35331-89-6

N-(2-Ethyl-2-hexenylidene)benzenamine, also known as EHBA, is a chemical compound with a molecular formula C18H23N. It is a type of aromatic amine and is commonly used as a reactant in the production of dyes and other organic compounds. EHBA has a molecular weight of 257.38 g/mol and is a clear, colorless liquid with a faint odor. It is considered to be stable under normal conditions, but may react violently with strong oxidizing agents.

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  • 35331-89-6 Structure

  • Basic information

    1. Product Name: N-(2-Ethyl-2-hexenylidene)benzenamine
    2. Synonyms: N-(2-Ethyl-2-hexenylidene)benzenamine
    3. CAS NO:35331-89-6
    4. Molecular Formula: C14H19N
    5. Molecular Weight: 201.3074
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 35331-89-6.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 301.1°Cat760mmHg
    3. Flash Point: 127.8°C
    4. Appearance: /
    5. Density: 0.86g/cm3
    6. Vapor Pressure: 0.00192mmHg at 25°C
    7. Refractive Index: 1.49
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: N-(2-Ethyl-2-hexenylidene)benzenamine(CAS DataBase Reference)
    11. NIST Chemistry Reference: N-(2-Ethyl-2-hexenylidene)benzenamine(35331-89-6)
    12. EPA Substance Registry System: N-(2-Ethyl-2-hexenylidene)benzenamine(35331-89-6)

  • 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: 35331-89-6(Hazardous Substances Data)

35331-89-6 Usage

Uses

Used in Chemical Industry:
N-(2-Ethyl-2-hexenylidene)benzenamine is used as a reactant for the production of dyes and other organic compounds, contributing to the synthesis of various chemical products.
Used in Dye Production:
N-(2-Ethyl-2-hexenylidene)benzenamine is used as a key component in the manufacturing process of dyes, providing the necessary chemical structure for color development and stability in various applications.
It is important to handle and store N-(2-Ethyl-2-hexenylidene)benzenamine with caution due to its potential for hazardous reactions with strong oxidizing agents.

Check Digit Verification of cas no

The CAS Registry Mumber 35331-89-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,3,3 and 1 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 35331-89:
(7*3)+(6*5)+(5*3)+(4*3)+(3*1)+(2*8)+(1*9)=106
106 % 10 = 6
So 35331-89-6 is a valid CAS Registry Number.
InChI:InChI=1/C14H19N/c1-3-5-9-13(4-2)12-15-14-10-7-6-8-11-14/h6-12H,3-5H2,1-2H3/b13-9-,15-12+

35331-89-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2-ethyl-2-hexen-1-ylidene)-Benzenamine

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:35331-89-6 SDS

35331-89-6Relevant articles and documents

Base-initiated oxidation of alkylindeneanilines by oxygen

Grigoryan, G. S.,Tovmasyan, V. S.,Malkhasyan, A. Ts.,Martirosyan, G. T.,Beletskaya, I. P.

, p. 50 - 56 (2007/10/02)

Oxidation and alkylation processes compete in the oxidative transformation of alkylindeneanilines in an alkaline medium.Oxidation leads mainly to the formation of formanilide anbd the corresponding carbonyl compound.Alkylation leads to a product which easily eliminates the aniline molecule with the formation of a derivative of the 1-aza-1,3-diene.A combination of alkylation and oxidation led to derivatives of quinoline.It is assumed that the alkylation-dehydrocyclization-elimination of alkylindeneanilines to quinolines by the action of oxygen and alkali is a variant of the Doebner-Miller reaction.During oxidation in the presence of sodium borohydride the products from conjugate oxidation-reductiono, i.e., the α-imino and β-amino alcohols, are also formed in addition to quinolines and oxidation and alkylation products.

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