(4,8-Bis(4-chloro-5-(2-ethylhexyl)thiophen-2-yl)benzo[1,2-b;4,5-b']dithiophene-2,6-diyl)bis(trimethylstannane) - Names and Identifiers
Name | (4,8-Bis(4-chloro-5-(2-ethylhexyl)thiophen-2-yl)benzo[1,2-b 4,5-b']dithiophene-2,6-diyl)bis(trimethylstannane)
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Synonyms | M7020 PM387 IN1776 BDTTH26CL-2SN IN1776, (4,8-Bis(4-chloro-5-(2-ethylhexyl)thiophen-2-yl)benzo[1,2-b (4,8-Bis(4-chloro-5-(2-ethylhexyl)thiophen-2-yl)benzo[1,2-b 4,5-b']dithiophene-2,6-diyl)bis(trimethylstannane)
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CAS | 2239295-69-1
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EINECS | 200-258-5 |
(4,8-Bis(4-chloro-5-(2-ethylhexyl)thiophen-2-yl)benzo[1,2-b;4,5-b']dithiophene-2,6-diyl)bis(trimethylstannane) - Physico-chemical Properties
Molecular Formula | C40H56Cl2S4Sn2
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Molar Mass | 973.46 |
Boling Point | 795.6±70.0 °C(Predicted) |
Appearance | Light yellow solid |
Odor | Light yellow crystals |
Storage Condition | 2-8°C |
(4,8-Bis(4-chloro-5-(2-ethylhexyl)thiophen-2-yl)benzo[1,2-b;4,5-b']dithiophene-2,6-diyl)bis(trimethylstannane) - Introduction
(4,8-bis (4-chloro-5-(2-ethylhexyl)thiophen-2-yl)benzo[1,2-b;4,5-b ']dithiophene-2,6-diyl)bis(trimethylstannane), is an organic compound, commonly abbreviated as Sn(S2C6H2(CH2S(CH3)2)Cl)2. The following is a description of the properties, uses, preparation and safety information of the compound:
Nature:
-Appearance: Yellow to orange solid.
-Solubility: Soluble in organic solvents, such as benzene, dimethylformamide, etc.
-Melting point: about 190-195 degrees Celsius.
Use:
-Catalyst: Sn(S2C6H2(CH2S(CH3)2)Cl)2 can be used as a catalyst in organic synthesis, with catalytic activity for redox and cross polycondensation reactions.
-Semiconductor material: The compound can be used to prepare organic semiconductor materials, such as organic solar cells and organic thin film transistors.
-Other uses: As a precursor for dyes, catalysts and antibacterial agents, it can also be used in the preparation of electronic materials and optical materials.
Preparation Method:
The method for preparing Sn(S2C6H2(CH2S(CH3)2)Cl)2 is relatively complicated and usually involves multi-step synthesis reactions. A common method of preparation is by nitration and ring-closing of benzylaminothiophene to obtain the desired product.
Safety Information:
-Because this compound has not been extensively studied, there are few relevant safety information data. However, as an organotin compound, it may have some properties of common organotin compounds, such as potential toxicity and potential impact on the environment. Therefore, appropriate laboratory safety practices should be followed during use and handling, including the wearing of safety gloves and goggles. At the same time, it is also recommended to operate in a well-ventilated place to avoid possible contact or inhalation.
Last Update:2024-04-09 21:04:16