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159709-36-1

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159709-36-1 Usage

General Description

3,4-DIMETHYLTHIENO[2,3-B]THIOPHENE-2-CARBALDEHYDE is a chemical compound with the molecular formula C9H8OS. It is a type of carbonyl compound, specifically an aldehyde, and is derived from the parent compound thienothiophene. This chemical is used in a variety of industrial applications, including as a building block for the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. It is known for its aromatic and sulfur-containing properties, and its structure allows for it to participate in various chemical reactions. Additionally, its structure and properties make it a valuable tool in organic synthesis and chemical research.

Check Digit Verification of cas no

The CAS Registry Mumber 159709-36-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,9,7,0 and 9 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 159709-36:
(8*1)+(7*5)+(6*9)+(5*7)+(4*0)+(3*9)+(2*3)+(1*6)=171
171 % 10 = 1
So 159709-36-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H8OS2/c1-5-4-11-9-8(5)6(2)7(3-10)12-9/h3-4H,1-2H3

159709-36-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4-dimethylthieno[2,3-b]thiophene-5-carbaldehyde

1.2 Other means of identification

Product number -
Other names 3,5-dimethyl thieno(2,3-b) thiophene 2-carboxaldehyde

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:159709-36-1 SDS

159709-36-1Downstream Products

159709-36-1Relevant articles and documents

Synthesis and structures of thieno[2,3-b]thiophene incorporated [3.3]dithiacyclophanes. Enhanced first hyperpolarizability in an unsymmetrically polarized cyclophane

Mashraqui, Sabir H.,Sangvikar, Yogesh S.,Meetsma, Auke

, p. 5599 - 5602 (2006)

Dithiacyclophanes incorporating thieno[2,3-b]thiophene have been synthesized, in order to investigate the nonlinear optical properties of donor-acceptor cyclophane 7. Cyclophane 7 displayed significantly higher first hyperpolarizability β (21.6 × 10-30 esu) compared to model 10 (9.58 × 10-30esu). Relatively higher β in 7 presumably arises from an extra electron redistribution arising from through-space charge transfer, a feature lacking in 10. Moreover, the thermal decomposition temperature of 7 (300 °C) is higher than that reported for the NLO prototype DANS (295 °C).

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