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2-(2,2-Dimethylpropyl)thiophene is an organic compound with the molecular formula C9H16S. It is a derivative of thiophene, a heterocyclic compound consisting of a benzene ring with one carbon atom replaced by a sulfur atom. The 2,2-dimethylpropyl group is attached to the thiophene ring at the 2-position, which is the carbon atom adjacent to the sulfur atom. 2-(2,2-Dimethylpropyl)thiophene is characterized by its unique chemical structure, which contributes to its distinct properties and potential applications in various fields, such as pharmaceuticals, agrochemicals, and materials science. Due to its specific functional groups and molecular structure, 2-(2,2-dimethylpropyl)thiophene may exhibit different reactivity and stability compared to other thiophene derivatives, making it an interesting subject for further research and development.

4891-29-6

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4891-29-6 Usage

Structure

A thiophene derivative with a 2,2-dimethylpropyl group attached to the thiophene ring

Usage

Commonly used as a building block in the synthesis of various organic compounds, including pharmaceuticals, agrochemicals, and materials

Potential applications

Studied for its potential applications in organic electronics and as a flavor and fragrance ingredient

Unique structure and reactivity

Makes it a valuable and versatile compound in the field of organic synthesis and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 4891-29-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,9 and 1 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4891-29:
(6*4)+(5*8)+(4*9)+(3*1)+(2*2)+(1*9)=116
116 % 10 = 6
So 4891-29-6 is a valid CAS Registry Number.

4891-29-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-neopentyl thiophene

1.2 Other means of identification

Product number -
Other names 2-(2,2-dimethylpropyl)thiophene

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:4891-29-6 SDS

4891-29-6Downstream Products

4891-29-6Relevant academic research and scientific papers

Transition metal complex, the dye and pigment-containing oxide semiconductor electrode and dye-sensitized solar cell

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, (2016/12/12)

PROBLEM TO BE SOLVED: To provide a transition metal complex which exhibits strong absorptions in a wide range of spectra and serves as a novel photosensitizer dye having excellent durability, as well as an oxide semiconductor electrode and a dye-sensitized solar cell that contain the dye. SOLUTION: The bivalent transition metal including (i) a bipyridyl polyacidic ligand such as a dicarboxybipyridyl (dcbpy) ligand as an adsorption site for adsorption onto the surface of titanium dioxide particles, (ii) a ligand which is selected from among isothiocyanato, isocyanato, and isoselenato groups and enables absorption excitation/charge transfer at long wavelengths, and (iii) a bipyridyl (bpy) ligand directly bonded to or conjugated to a five-membered heterocyclic ring having an alkyl, an alkoxyalkyl, or an alkoxy group including a quaternary carbon atom which may be optionally substituted by one or more fluoro groups for providing nucleophilic reagent stability to a sensitizer dye to improve the absorbance and bathochromic effect in absorption of the transition metal complex, and the photosensitizer dye having the structure are provided. COPYRIGHT: (C)2011,JPOandINPIT

TETRACYCLIC COMPOUNDS AS DOPAMINE AGONISTS

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, (2008/06/13)

A tetracyclic compound of the formula: STR1 wherein A and the atoms to which it is attached and the optional double bond represent a mono-or di-heterocyclic ring selected from: STR2 wherein R 1, R. sup.2, R 3, R 4 and X are specifically defined, which compounds are useful in the treatment of dopamine-related neurological, psychological and cardiovascular disorders as well as in the treatment of substance abuse and other addictive behavior disorders, cognitive impairment and attention deficit disorder.

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