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35331-89-6

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35331-89-6 Usage

General Description

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. EHBA is primarily used in industrial applications, but it is important to handle and store it with caution due to its potential for hazardous reactions.

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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