Welcome to LookChem.com Sign In|Join Free
  • or
2,2'-BITHIOPHENE-5-METHYLAMINE is a chemical compound that belongs to the bithiophene family, characterized by its fused ring structures containing two thiophene rings. It is a substituted derivative with a methylamine group attached to the 5-position of one of the thiophene rings, which endows it with unique properties and potential applications in various fields.

4380-96-5

Post Buying Request

4380-96-5 Suppliers

Recommended suppliers

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

4380-96-5 Usage

Uses

Used in Organic Electronics:
2,2'-BITHIOPHENE-5-METHYLAMINE is used as a building block for the synthesis of organic semiconductors and conductive polymers, due to its unique structure and properties that contribute to the development of advanced materials in this field.
Used in Materials Science:
In the field of materials science, 2,2'-BITHIOPHENE-5-METHYLAMINE is utilized for the development of new materials for electronic and optoelectronic devices, such as organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs), owing to its potential to enhance the performance and efficiency of these devices.
Used in Electronic Device Development:
2,2'-BITHIOPHENE-5-METHYLAMINE is employed in the development of new materials for electronic devices, with the aim of improving their efficiency and sustainability. Its unique structure and properties make it a promising candidate for advancing the production of more efficient electronic technologies.

Check Digit Verification of cas no

The CAS Registry Mumber 4380-96-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,8 and 0 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4380-96:
(6*4)+(5*3)+(4*8)+(3*0)+(2*9)+(1*6)=95
95 % 10 = 5
So 4380-96-5 is a valid CAS Registry Number.

4380-96-5SDS

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 (5-thiophen-2-ylthiophen-2-yl)methanamine

1.2 Other means of identification

Product number -
Other names 2,2'-bithiophen-5-ylmethanamine

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:4380-96-5 SDS

4380-96-5Relevant academic research and scientific papers

One-pot primary aminomethylation of aryl and heteroaryl halides with sodium phthalimidomethyltrifluoroborate

Murai, Norio,Miyano, Masayuki,Yonaga, Masahiro,Tanaka, Keigo

, p. 2818 - 2821 (2012/07/17)

A one-pot primary aminomethylation of aryl halides, triflates, mesylates, and tosylates via Suzuki-Miyaura cross-coupling reactions with sodium phthalimidomethyltrifluoroborate followed by deamidation with ethylenediamine is reported.

Novel cyclopentane dicarboxamide sodium channel blockers as a potential treatment for chronic pain

Shao, Pengchang P.,Ok, Dong,Fisher, Michael H.,Garcia, Maria L.,Kaczorowski, Gregory J.,Li, Chunshi,Lyons, Kathryn A.,Martin, William J.,Meinke, Peter T.,Priest, Birgit T.,Smith, McHardy M.,Wyvratt, Matthew J.,Ye, Feng,Parsons, William H.

, p. 1901 - 1907 (2007/10/03)

A series of new voltage-gated sodium channel blockers were prepared based on the screening lead succinic diamide BPBTS. Replacement of the succinimide linker with the more rigid cyclic 1,2-trans-diamide linker was well tolerated. N-Methylation on the biph

1,2 DIAMIDO CYCLOALKYL SODIUM CHANNEL BLOCKERS

-

, (2010/11/30)

1,2 Diamido cycloalkyl compounds that are sodium channel blockers; pharmaceutical compositions that include an effective amount of the aryl-link-aryl thiazolidin-dione and aryl-link-aryl oxazolodine-dione compounds and a pharmaceutically acceptable carrier; and a method of treatment of acute pain, chronic pain, visceral pain, inflammatory pain, or neuropathic pain, as well as irritable bowel syndrome, Crohns disease, epilepsy, partial and generalized tonic seizures, multiple sclerosis, bipolar disease, and tachy-arrhythmias by the administration of an effective amount of aryl-link-aryl thiazolidine-dione and aryl-link-aryl oxazolodine-dione compounds, either alone, or in combination with one or more therapeutically active compounds, are described.

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 4380-96-5