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5′-己基-2,2′-联噻吩-5-硼酸频哪醇酯_分子结构_CAS_579503-59-6)
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5′-己基-2,2′-联噻吩-5-硼酸频哪醇酯

产品号 632961 公司名称 Sigma Aldrich
CAS号 579503-59-6 公司网站 http://www.sigmaaldrich.com
分子式 C20H29BO2S2 电 话 1-800-521-8956
分子量 376.38406 传 真
纯 度 97% 电子邮件
保 存 Chembase数据库ID: 141731

产品价格信息

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产品别名

标题
5′-Hexyl-2,2′-bithiophene-5-boronic acid pinacol ester
IUPAC标准名
2-[5-(5-hexylthiophen-2-yl)thiophen-2-yl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
IUPAC传统名
2-[5-(5-hexylthiophen-2-yl)thiophen-2-yl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
别名
5′-N-己基-2,2′-联噻吩-5-硼酸频哪醇酯
5-(4,4,5,5-四甲基-1,3,2-二氧杂硼烷-2-基)-5′-N-己基-2,2′-联噻吩
5-己基-5′-(4,4,5,5-四甲基-1,3,2-二氧杂硼烷-2-基)-2,2′-联噻吩
5-Hexyl-5′-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2,2′-bithiophene
2-(5′-Hexyl-2,2′-bithien-5-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
4,4,5,5-Tetramethyl-2-[5′-hexyl-2,2′-bithien-5-yl]-1,3,2-dioxaborolane
5′-N-Hexyl-2,2′-bithiophene-5-boronic acid pinacol ester
5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-5′-N-hexyl-2,2′-bithiophene

产品登记号

MDL号 MFCD05664380
CAS号 579503-59-6
PubChem SID 24882530

产品性质

Empirical Formula (Hill Notation) C20H29BO2S2
纯度 97%
熔点 36-40 °C(lit.)
GHS危险品标识 GHS07
GHS警示词 Warning
GHS危险声明 H302
欧盟危险性物质标志 有害性(Harmful) 有害性(Harmful) (Xn)
MSDS下载 下载链接
个人保护装置 dust mask type N95 (US), Eyeshields, Gloves
危险公开号 22
安全公开号 36
德国WGK号 3

产品详细信息

详细说明 (English)
Packaging
1, 5 g in glass bottle
Application
Reagent use for
• Suzuki-Miyaura cross-coupling reactions and shape-shifting in contorted dibenzotetrathienocoronenes1
• Oligothiophene self-assembly induction into fibers with tunable shape and function2
• Stille coupling and p-conjugated packing structure and hole mobility of bithiophene-bithiazole copolymers with alkyl-thiophene side chains3 Reagent used in Preparation of
• Solution-processed ambipolar field-effect transistor4
• Light harvesting small molecules for use in solution-processed small molecule bulk heterojunction solar cell devices5
• Light-emitting diode (OLED) materials6
• Unsymmetric substituted benzothiadiazole-containing vinyl monomers for RAFT polymerization7
• Pd-catalyzed condensations and synthesis of isoindigo-based oligothiophenes for molecuar bulk heterojunction solar cells8
• Thiophene-benzothiadiazole based donor-acceptor-donor materials9
详细说明 (简体中文)
包装
1, 5 g in glass bottle
Application
Reagent use for
• Suzuki-Miyaura cross-coupling reactions and shape-shifting in contorted dibenzotetrathienocoronenes1
• Oligothiophene self-assembly induction into fibers with tunable shape and function2
• Stille coupling and p-conjugated packing structure and hole mobility of bithiophene-bithiazole copolymers with alkyl-thiophene side chains3 Reagent used in Preparation of
• Solution-processed ambipolar field-effect transistor4
• Light harvesting small molecules for use in solution-processed small molecule bulk heterojunction solar cell devices5
• Light-emitting diode (OLED) materials6
• Unsymmetric substituted benzothiadiazole-containing vinyl monomers for RAFT polymerization7
• Pd-catalyzed condensations and synthesis of isoindigo-based oligothiophenes for molecuar bulk heterojunction solar cells8
• Thiophene-benzothiadiazole based donor-acceptor-donor materials9

参考文献