178934
三氯化硼 溶液
1.0 M in methylene chloride
别名:
Boron chloride, Trichloroborane
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关于此项目
经验公式（希尔记法）:
BCl3
化学文摘社编号:
分子量:
117.17
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352106
MDL number:
Quality Level
vapor pressure
29.72 psi ( 55 °C), 9.05 psi ( 20 °C)
form
liquid
reaction suitability
core: boron, reagent type: Lewis acid, reagent type: catalyst
concentration
1.0 M in methylene chloride
density
1.326 g/mL at 25 °C
storage temp.
2-8°C
SMILES string
ClB(Cl)Cl
InChI
1S/BCl3/c2-1(3)4
InChI key
FAQYAMRNWDIXMY-UHFFFAOYSA-N
General description
Boron trichloride is a boron halide. It participates in the hydroboration of alkenes. It forms strongly polarized donor-acceptor complexes with trimethyl- and triethylsilyl triflate. Boron trichloride assisted reaction between acid chlorides and alkynyltrifluoroborate salts have been reported to form ynones.
Boron trichloride solution is used as a Lewis acid catalyst in the synthesis of BN-phenanthrenes.
Boron trichloride solution is used as a Lewis acid catalyst in the synthesis of BN-phenanthrenes.
Application
Boron trichloride may be used in the synthesis of Cl-BODIPYs (BODIPY - Boron-dipyrromethene) and tris(dimethylamino)borane. It may be used in the synthesis of sceptrins and nakamuric acid.
用于制备脂肪酸甲酯以及用于三酸甘油酯的酯交换反应。
Packaging
The 25 mL Sure/Seal™ bottle is recommended as a single-use bottle. Repeated punctures will likely result in decreased performance of product.
Legal Information
Sure/Seal is a trademark of Sigma-Aldrich Co. LLC
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Danger
Hazard Classifications
Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Carc. 2 - Eye Dam. 1 - Repr. 1B - Skin Corr. 1B - STOT SE 3
target_organs
Central nervous system
存储类别
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
监管及禁止进口产品
此项目有
Xiaolei Wang et al.
Organic chemistry frontiers : an international journal of organic chemistry, 2(8), 978-984 (2015-09-04)
Sceptrins and nakamuric acid are structurally unique antibiotics isolated from marine sponges. Recent studies suggest that the biosynthesis of these dimeric pyrrole-imidazole alkaloids involves a single-electron transfer (SET)-promoted [2+2] cycloaddition to form their cyclobutane core skeletons. We describe herein the
A New Member of the BN-Phenanthrene Family: Understanding the Role of the B?N Bond Position
Abengo?zar, Alberto and Sucunza
The Journal of Organic Chemistry, 84, 7113-7122 (2019)
Synthesis of highly electrically conductive and electrochemically stable porous boron-doped carbon microspheres
Bose, Anima B and Yang, et al.
SN Applied Sciences, 1, 1-8 (2019)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 178934-800ML | 04061838754066 |
| 178934-100ML | 04061838754035 |
| 178934-25ML | 04061838083890 |
| 178934-2L | 04061838754042 |
| 178934-4X25ML | 04061838754059 |