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88686-98-0

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88686-98-0 Usage

Family

Dithiophene derivatives

Type of Compound

Heterocyclic compound

Core Structure

Benzo[c]dithiophene

Fused Rings

Two

Oxygen Atoms

Two

Structure

Unique with potential electronic and optical properties

Application

Organic electronics

Subfields

Organic photovoltaics, light-emitting diodes, and field-effect transistors

Properties

Favorable electron-donating and conducting properties

Significance

Interesting candidate for research and development in organic semiconductors

Check Digit Verification of cas no

The CAS Registry Mumber 88686-98-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,6,8 and 6 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 88686-98:
(7*8)+(6*8)+(5*6)+(4*8)+(3*6)+(2*9)+(1*8)=210
210 % 10 = 0
So 88686-98-0 is a valid CAS Registry Number.

88686-98-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3,6,8-tetrahydrothieno[3,4-g][2]benzothiole 2,7-dioxide

1.2 Other means of identification

Product number -
Other names Benzo[1,2-c:3,4-c']dithiophene,1,3,6,8-tetrahydro-,2,7-dioxide (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:88686-98-0 SDS

88686-98-0Relevant articles and documents

Improved Synthesis and Electrophilic Bromination of Benzodithiophene. Charge-Transfer and Cycloaddition Reaction with Tetracyanoethylene

Lin, Lon-Tang Wilson,Hart, Harold

, p. 1027 - 1030 (2007/10/02)

Benzodithiophene (6) is prepared in two steps and 47percent overall yield from its tetrahydro precursor 7.Bromination of 6 ( NBS, AcOH) occurs in the thiophene moities; preparation of the 1-Br, 3-Br, 1,3-Br2, 1,3,6-Br3, 1,3,6,8-Br4, and 1,3,

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