Welcome to LookChem.com Sign In|Join Free
  • or
4-[(4-dimethylaminophenyl)-thiophen-2-yl-methyl]-N,N-dimethyl-aniline is a complex organic compound with the molecular formula C21H24N2S. It is characterized by a central aniline group (C6H5NH2), which is substituted at the 4-position with a thiophen-2-yl-methyl group. This thiophen-2-yl-methyl group is further connected to a 4-dimethylaminophenyl group, which itself is a phenyl ring (C6H5) with two methyl groups (CH3) attached to the nitrogen atom. The entire structure is symmetrically dimethylated on the nitrogen atom of the central aniline group. 4-[(4-dimethylaminophenyl)-thiophen-2-yl-methyl]-N,N-dimethyl-aniline is likely to be used in the synthesis of dyes, pigments, or as an intermediate in the production of various pharmaceuticals and chemical compounds due to its unique structure and potential reactivity.

6339-91-9

Post Buying Request

6339-91-9 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

6339-91-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6339-91-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,3 and 9 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6339-91:
(6*6)+(5*3)+(4*3)+(3*9)+(2*9)+(1*1)=109
109 % 10 = 9
So 6339-91-9 is a valid CAS Registry Number.

6339-91-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[[4-(dimethylamino)phenyl]-thiophen-2-ylmethyl]-N,N-dimethylaniline

1.2 Other means of identification

Product number -
Other names Thiophengruen

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:6339-91-9 SDS

6339-91-9Downstream Products

6339-91-9Relevant academic research and scientific papers

Spectral Properties of Fluorogenic Thiophene-derived Triarylmethane Dyes

Stensrud, Kenneth F.,Zanotti, Kimberly J.,Waggoner, Alan S.,Armitage, Bruce A.

, p. 406 - 410 (2018/11/27)

Spectral properties and fluorogenic behaviors of five novel thiophene variants of malachite green (MG), termed MGTs, were determined. Appreciable changes as a function of homologation and substitution pattern, including absorption band positions and inten

Efficient synthesis of Bis(4-Dimethaminophenyl)arylmethanes and Bis(4-Diamethaminophenyl)alkanes using iodine reagent

Bachhav, Harshal M.,Takale, Balaram S.,Telvekar, Vikas N.

, p. 1909 - 1914 (2013/05/21)

A novel synthetic utility of NaICl2 for the preparation of bis(4-dimethaminophenyl)arylmethanes and bis(4-dimethaminophenyl)alkanes is described. In the presence of an aqueous solution of NaICl2, the reaction of arenes with aromatic aldehydes gives corresponding triarylmethane derivatives regioselectively in moderate to good yields. The method is also useful for the preparation of diarylalkane derivatives by using aliphatic aldehydes. Supplemental materials are available for this article. Go to the publisher's online edition of Synthetic Communications to view the free supplemental file.

SbCl3-catalyzed one-pot synthesis of 4,4′-diamino- triarylmethanes under solvent-free conditions: Synthesis, characterization, and DFT studies

Bardajee, Ghasem Rezanejade

experimental part, p. 135 - 144 (2011/05/16)

A simple, efficient, and mild procedure for a solvent-free one-step synthesis of various 4,4′-diaminotriarylmethane derivatives in the presence of antimony trichloride as catalyst is described. Triarylmethane derivatives were prepared in good to excellent yields and characterized by elemental analysis, FTIR, 1H and 13C NMR spectroscopic techniques. The structural and vibrational analysis were investigated by performing theoretical calculations at the HF and DFT levels of theory by standard 6-31Gs *, 6-31G*/B3LYP, and B3LYP/cc-pVDZ methods and good agreement was obtained between experimental and theoretical results.

Montmorillonite K10 clay catalysed Baeyer condensation of heterocyclic aldehydes with N,N-dimethylaniline: Synthesis and photo irradiation studies of heteroaryldiarylmethanes

Shanmuga,Varma

, p. 1258 - 1263 (2007/10/03)

The montmorillonitemK10 clay catalysed Baeyer condensation of a number of aromatic heterocyclic aldehydes (1-7) with N,N-dimethylaniline affords novel triarylmethanes (8-14) in good yield. The triarylmethane 8 was irradiated at 325 nm for 1 hr under different solvent systems and the photoproducts were identified as 15 and 16.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 6339-91-9