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N,N-diethyl-N-methylanilinium, also known as N,N-diethyl-N-methylbenzenaminium, is an organic compound with the chemical formula C11H18N. It is a derivative of aniline, where the hydrogen atoms on the nitrogen atom are replaced by diethyl and methyl groups, resulting in a quaternary ammonium salt. N,N-diethyl-N-methylanilinium is a colorless, crystalline solid that is soluble in water and organic solvents. It is used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. Due to its cationic nature, N,N-diethyl-N-methylanilinium can also be used as a phase-transfer catalyst in organic reactions.

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  • 1007-67-6 Structure
  • Basic information

    1. Product Name: N,N-diethyl-N-methylanilinium
    2. Synonyms:
    3. CAS NO:1007-67-6
    4. Molecular Formula: C11H18N*I
    5. Molecular Weight: 164.2668
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1007-67-6.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: N,N-diethyl-N-methylanilinium(CAS DataBase Reference)
    10. NIST Chemistry Reference: N,N-diethyl-N-methylanilinium(1007-67-6)
    11. EPA Substance Registry System: N,N-diethyl-N-methylanilinium(1007-67-6)
  • 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: 1007-67-6(Hazardous Substances Data)

1007-67-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1007-67-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,0 and 7 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1007-67:
(6*1)+(5*0)+(4*0)+(3*7)+(2*6)+(1*7)=46
46 % 10 = 6
So 1007-67-6 is a valid CAS Registry Number.

1007-67-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name diethyl-methyl-phenylazanium,iodide

1.2 Other means of identification

Product number -
Other names Diethylmethylphenylammonium iodid

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:1007-67-6 SDS

1007-67-6Relevant articles and documents

Carbonylation of quaternary ammonium salts to tertiary amides using NaCo(CO)4 catalyst

Lei, Yizhu,Zhang, Rui,Wu, Qing,Mei, Hui,Xiao, Bo,Li, Guangxing

, p. 120 - 125 (2014)

We reported here the catalytic carbonylation of quaternary ammonium salts under anhydrous condition. Quaternary ammonium salts, a kind of versatile reagents that were widely used in organometallic chemistry, can be carbonylated to tertiary amides by an in situ prepared NaCo(CO)4 catalyst. It was found that the counterions (Cl-, Br-, I-, OTf-) in the quaternary ammonium salts played a significant role in the reaction and tetramethylammonium iodide could give high yield (96%) of N,N-dimethylacetamide (DMAc) with only 0.5 mol% cobalt catalyst. Under optimum conditions, several other quaternary ammonium iodides were also carbonylated to corresponding tertiary amides in moderate to excellent yields. Obviously, these results also give us a special apprehension that Me4NI and other quaternary ammonium salts could be possibly carbonylated to tertiary amides in the carbonylation reaction where they are used as promoters or solvents in most cases. Considering the high activity and moderate to excellent selectivity, this process could be a potential method for the synthesis of certain tertiary amides. Moreover, the cleaving mechanism of CN bonds and the possible catalytic intermediates were discussed in detail.

Wedekind-Fock-Havinga salt Me(Et)N+(All)PhI- · CHCl3 as historically the first object for absolute asymmetric synthesis: Spontaneous resolution, structure and absolute configuration

Kostyanovsky,Kostyanovsky,Kadorkina,Lyssenko

, p. 1 - 5 (2001)

The title salt crystallises as a conglomerate (space group P212121, Z = 4) with one solvate CHCl3 molecule forming strong shortened contact with I- [Cl···I- 3.599(2) A?]. Therefore, it unde

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