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4-IODO-2,1,3-BENZOTHIADIAZOLE is a synthetic organosulfur compound characterized by the presence of iodine. It is a member of the benzothiadiazol class and is widely recognized for its role as a building block in the synthesis of organic semiconductors. This chemical compound is particularly valuable in the development of conjugated polymers and small molecules for applications in organic light-emitting diodes (OLEDs) and organic photovoltaics. The iodine atoms within its molecular structure offer opportunities for further functionalization, which can alter and improve the compound's properties. The physical characteristics of 4-IODO-2,1,3-BENZOTHIADIAZOLE, such as color, solubility, melting, or boiling point, may vary depending on the specific derivative compounds. Safe storage and handling are essential, and considerations regarding its toxicity and ecological impact must be adhered to in accordance with chemical handling regulations and practices.

352018-95-2

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352018-95-2 Usage

Uses

Used in Organic Semiconductor Synthesis:
4-IODO-2,1,3-BENZOTHIADIAZOLE is used as a building block for the synthesis of organic semiconductors, which are crucial in the development of advanced electronic materials. Its role in this application is to provide a foundation for the creation of conjugated polymers and small molecules that are essential for the performance of electronic devices.
Used in OLED Technology:
In the field of organic light-emitting diodes (OLEDs), 4-IODO-2,1,3-BENZOTHIADIAZOLE is utilized as a key component in the synthesis of materials that contribute to the light-emitting properties of OLEDs. Its presence in these materials can influence the efficiency, color, and stability of the emitted light, making it an important factor in the design and performance of OLED displays and lighting systems.
Used in Organic Photovoltaics:
4-IODO-2,1,3-BENZOTHIADIAZOLE is employed in the development of materials for organic photovoltaics, where it plays a role in enhancing the light absorption and charge transport properties of the photovoltaic cells. Its use in this application contributes to the overall efficiency and performance of solar energy conversion devices.
Used in Chemical Functionalization:
The iodine atoms in 4-IODO-2,1,3-BENZOTHIADIAZOLE molecules are often used for further functionalization, allowing for the modification and enhancement of the compound's properties. This application is crucial in the development of new materials with tailored characteristics for specific uses in various industries, such as electronics, pharmaceuticals, and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 352018-95-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,2,0,1 and 8 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 352018-95:
(8*3)+(7*5)+(6*2)+(5*0)+(4*1)+(3*8)+(2*9)+(1*5)=122
122 % 10 = 2
So 352018-95-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H3IN2S/c7-4-2-1-3-5-6(4)9-10-8-5/h1-3H

352018-95-2SDS

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 4-IODO-2,1,3-BENZOTHIADIAZOLE

1.2 Other means of identification

Product number -
Other names 2,1,3-Benzothiadiazole,4-iodo

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:352018-95-2 SDS

352018-95-2Upstream product

352018-95-2Downstream Products

352018-95-2Relevant academic research and scientific papers

Functionalization of the benzo[c][1,2,5]thiadiazole scaffold via Mg-, Zn- and Mn-intermediates

Zimdars, Silvia,Langhals, Heinz,Knochel, Paul

experimental part, p. 1302 - 1308 (2011/05/14)

The metalation of all positions of the benzo[c][1,2,5]thiadiazole scaffold using LiCl-solubilized TMP-bases is demonstrated on various substrates. Thus, unsymmetrically substituted benzothiadiazole derivatives and a new fused thiadiazoloindazole have been

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