35203-08-8

Basic information

• Product Name: Benzenamine, 2,6-diethyl-N-methylene-
• Synonyms: Benzenamine, 2,6-diethyl-N-methylene-;2,6-Diethyl-N-methylenebenzenamine;N-(2,6-Diethylphenyl)methanimine
• CAS NO: 35203-08-8
• Molecular Formula: C₁₁H₁₅N
• Molecular Weight: 161.24
• Mol File: 35203-08-8.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 275.3°Cat760mmHg
• Flash Point: 112.1°C
• Appearance: /
• Density: 0.88g/cm³
• Vapor Pressure: 0.0086mmHg at 25°C
• Refractive Index: 1.492
• CAS DataBase Reference: Benzenamine, 2,6-diethyl-N-methylene-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, 2,6-diethyl-N-methylene-(35203-08-8)
• EPA Substance Registry System: Benzenamine, 2,6-diethyl-N-methylene-(35203-08-8)

Safety Data

• Hazardous Substances Data: 35203-08-8(Hazardous Substances Data)

Usage

InChI:InChI=1/C11H15N/c1-4-9-7-6-8-10(5-2)11(9)12-3/h6-8H,3-5H2,1-2H3

Upstream product

• 59983-55-0 triethylammonium piperidinodithiocarbamate 
• 59983-58-3 pyrrolidine-1-carbodithioate triethylammonium 
• 579-66-8 2,6-diethylaniline 
• 50-00-0 formaldehyd 

Downstream Products

• 40164-96-3 2-Chloro-N-(2,6-diethyl-phenyl)-N-ureidomethyl-acetamide 
• 166407-15-4 2-Acetoxy-N-(2,6-diethylphenyl)-N-(methoxymethyl)acetamide 
• 40164-69-0 N-(chloromethyl)-2',6'-diethyl-2-chloroacetanilide 
• 113708-00-2 5-chloro-2-benzothiazolyl-N-(5-chloro-2-benzothiazolylthiomethyl)-2,6-diethylthiolcarbanilate 
• 113707-98-5 2-benzothiazolyl-N-(2-benzothiazolylthiomethyl)-2,6-diethylthiolcarbanilate 
• 113707-99-6 2-benzoxazolyl-N-(2-benzoxazolylthiomethyl)-2,6-diethylthiolcarbanilate 
• 113708-02-4 4,6-dimethyl-2-pyrimidinyl-N-(2,6-diethylphenyl)-N-(4,6-dimethyl-2-pyrimidinylthiomethyl)thiolcarbanilate 
• 113708-03-5 3-(2,6-diethylphenyl)-3,4-dihydro-2H-<1,3,5>thiadiazino<3,2-a>benzimidazol-2-one 
• 74886-79-6 N-(2,6-Diethylphenyl)-N-(methoxymethyl)acetamide 
• 579-66-8 2,6-diethylaniline 
• 24544-05-6 N-methyl-N-(2,6-diethylphenyl)amine 
• 2909-78-6 N,N-dimethyl-2,6-diethylaniline 
• 68950-93-6 N-benzyl-2,6-diethylaniline 
• 122-39-4 diphenylamine 

Relevant articles and documents

Occurrence of alachlor environmental degradation products in groundwater

Groundwater samples collected beneath a Massachusetts corn field were analyzed by gas chromatography/mass spectrometry. In addition to alachlor, 20 compounds were detected whose EI and CIMS data indicated that they were derived from alachlor, presumably via environmental degradation. Structural assignments were confirmed for six of these compounds by analysis of standards. They were among 10 alachlor-related compounds that were synthesized by use of either the parent compound or 2,6-diethylaniline as starting material. -from Authors

HOMOLYTIC ADDITION OF 1,4-DIOXANE TO SCHIFF BASES

Radical addition of 1,4-dioxane to aldimines proceeds at the imidyl carbon atom with formation of asymmetrical secondary amines.By the method of competitive kinetics we have determined the relative activities of Schiff bases and have found that the regiod

Synthesis of N-(Chloromethyl)-2,6-diethylcarbaniloyl Chloride (1) and Derivatives

The reaction of N-methylene-2,6-diethylbenzenamine with phosgene furnished the titled compound 1.The reaction of 1 with the potassium salts of thiazolethiols in an acetone medium afforded the expected N-substituted 2,6-diethylthiolcarbanilates 2-6.Substit