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23290-55-3

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23290-55-3 Usage

General Description

2-t-Butoxythiophene is a chemical compound with the molecular formula C10H14OS. It is a thiophene derivative with a t-butoxy group attached to the 2-position of the thiophene ring. 2-t-Butoxythiophene is commonly used in the synthesis of organic materials such as polymers, liquid crystals, and organic electronics. 2-t-Butoxythiophene is known for its high thermal stability and electrical conductivity, making it a valuable building block for various electronic applications. It is also used as a building block in the production of dyes and pigments. Additionally, 2-t-Butoxythiophene has potential applications in the pharmaceutical industry and is being studied for its biological activities.

Check Digit Verification of cas no

The CAS Registry Mumber 23290-55-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,2,9 and 0 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 23290-55:
(7*2)+(6*3)+(5*2)+(4*9)+(3*0)+(2*5)+(1*5)=93
93 % 10 = 3
So 23290-55-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H12OS/c1-8(2,3)9-7-5-4-6-10-7/h4-6H,1-3H3

23290-55-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(2-methylpropan-2-yl)oxy]thiophene

1.2 Other means of identification

Product number -
Other names 2-T-BUTOXYTHIOPHENE

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:23290-55-3 SDS

23290-55-3Relevant articles and documents

Addition of 2-tert-butyldimethylsilyloxythiophene to activated quinones: An approach to thia analogues of kalafungin

Brimble, Margaret A.,Laita, Olivia,Robinson, James E.

, p. 3021 - 3027 (2006)

The uncatalyzed reaction of 2-tert-butyldimethylsilyloxythiophene 2 with 1,4-quinones bearing either an electron withdrawing acetyl or a carbomethoxy group at C-2, was investigated. No reaction was observed using 1,4-quinones 8 and 9 bearing an ester grou

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