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1H,3H-Thieno[3,4-c]thiophene(7CI,8CI,9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

250-35-1

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250-35-1 Usage

Structure

Bicyclic compound with two fused thiophene rings

Aromaticity

Aromatic sulfur-containing compound

Organic electronic devices

Organic field-effect transistors and organic light-emitting diodes

Organic semiconductors

Due to favorable electronic properties and high thermal stability

Pharmaceutical and agrochemical development

As a building block for new compounds

Versatility

Wide range of potential applications in various industries

Check Digit Verification of cas no

The CAS Registry Mumber 250-35-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,5 and 0 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 250-35:
(5*2)+(4*5)+(3*0)+(2*3)+(1*5)=41
41 % 10 = 1
So 250-35-1 is a valid CAS Registry Number.

250-35-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-dihydrothieno[3,4-c]thiophene

1.2 Other means of identification

Product number -
Other names 1H,3H-Thieno[3,4-c]thiophene(7CI,8CI,9CI)

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:250-35-1 SDS

250-35-1Downstream Products

250-35-1Relevant academic research and scientific papers

Synthesis and reactivity of dipropargylic disulfides: tandem rearrangements, cyclization, and oxidative dimerization

Braverman, Samuel,Cherkinsky, Marina,Meridor, David,Sprecher, Milon

scheme or table, p. 1925 - 1930 (2010/04/24)

Synthesis and facile rearrangement and cyclization reaction of new dipropargylic disulfides are described. A possible mechanism for these transformations involving an initial double [2,3]-sigmatropic rearrangement to the elusive diallenyl disulfides via a thiosulfoxide intermediates is suggested.

REDUCTION DES CONTRAINTES STERIQUES (EMPECHEMENT A LA CONJUGAISON) DANS LES POLY(DIALKYL-3,4-THIOPHENES)

Garreau, R.,Roncali, J.,Garnier, F.,Lemaire, M.

, p. 93 - 98 (2007/10/02)

Cyclopenta thiophene, cyclopenta thiophene and thieno thiophene have been synthesized.The electropolymerization of these monomers was attempt.The electrical properties of poly(cyclopenta thiophene) are intermediate between those of poly(3-methylthiophene) and poly(3,4-dimethyl thiophene).

Generation and Characterization of the Parent 2λ4?2-Thienothiophene

Nakayama, Juzo,Ishii, Akihiko,Kobayashi, Yasunobu,Hoshino, Masamatsu

, p. 959 - 960 (2007/10/02)

The parent 2λ4?2-thienothiophene was generated by Pummerer dehydration of 1H,3H-thienothiophene 2-oxide and characterized by chemical trapping experiments.

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