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110851-66-6

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110851-66-6 Usage

Chemical Properties

Light yellow liquid

Uses

3-Tetradecylthiophene is a reactant used in the synthesis of 3''-alkyl-α-terthiophene derivatives with nematocidal activity.

Check Digit Verification of cas no

The CAS Registry Mumber 110851-66-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,8,5 and 1 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 110851-66:
(8*1)+(7*1)+(6*0)+(5*8)+(4*5)+(3*1)+(2*6)+(1*6)=96
96 % 10 = 6
So 110851-66-6 is a valid CAS Registry Number.
InChI:InChI=1/C18H32S/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-18-15-16-19-17-18/h15-17H,2-14H2,1H3

110851-66-6 Well-known Company Product Price

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  • TCI America

  • (T3104)  3-Tetradecylthiophene  >98.0%(GC)

  • 110851-66-6

  • 5g

  • 830.00CNY

  • Detail
  • TCI America

  • (T3104)  3-Tetradecylthiophene  >98.0%(GC)

  • 110851-66-6

  • 25g

  • 2,860.00CNY

  • Detail

110851-66-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Tetradecylthiophene

1.2 Other means of identification

Product number -
Other names Thiophene,3-tetradecyl

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:110851-66-6 SDS

110851-66-6Relevant articles and documents

Iron-catalyzed cross-coupling reactions of alkyl-Grignard reagents with aryl chlorides, tosylates, and triflates

Fuerstner, Alois,Leitner, Andreas

, p. 609 - 612 (2002)

Aryl chlorides are better substrates than the corresponding bromides or iodides in the presented cross-coupling with alkyl Grignard reagents that is catalyzed by iron salts (see scheme); even aryl tosylates are converted efficiently. This situation is att

Dithiophene based X-shaped bolaamphiphiles: Liquid crystals with single wall honeycombs and geometric frustration

Gao, Hongfei,Ye, Yafei,Kong, Leiyang,Cheng, Xiaohong,Prehm, Marko,Ebert, Helgard,Tschierske, Carsten

, p. 10921 - 10931,11 (2020/09/15)

A series of 5,5′-diphenyl-2,2′-dithiophene based X-shaped polyphiles with two long lateral alkyl chains and terminal glycerol groups was synthesized and the liquid crystalline phases formed by these compounds were investigated by polarizing microscopy, DSC and XRD. These compounds form square (p4mm and p4gm) and hexagonal (p6mm) columnar LC phases. In these mesophases the molecules organize into polygonal honeycombs where the π-conjugated cores form the walls, fused at the edges by the hydrogen bonding networks between the glycerol units and filled by the lateral alkyl chains. By elongation of these chains, a series of polygonal honeycomb phases with a "single wall" structure, ranging from triangular via square and pentagonal to hexagonal was observed. Most triangular honeycombs appear to be defective and can be considered as mixtures of triangular cylinders with orientationally randomized rhombic cylinders. The transition from this improper triangular honeycomb to the square honeycomb takes place via a disordered isotropic phase. Addition of water to this isotropic phase gives rise to a true triangular honeycomb LC phase. Replacing one of the long lateral chains by a small methyl group leads to honeycombs formed by double walls instead of single walls. UV investigations indicate π-stacking of the aromatic cores organized in the honeycomb walls, which is of interest for the potential application of these materials in self assembled arrays of organic electronic material. This journal is

Iron-catalyzed cross-coupling reactions

Fuerstner, Alois,Leitner, Andreas,Mendez, Maria,Krause, Helga

, p. 13856 - 13863 (2007/10/03)

Simple iron salts such as FeCln, Fe(acac)n (n = 2,3) or the salen complex 4 turned out to be highly efficient, cheap, toxicologically benign, and environmentally friendly precatalysts for a host of cross-coupling reactions of alkyl o

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