추천 제품
Quality Level
분석
96%
형태
liquid
반응 적합성
core: boron
reagent type: Lewis acid
reagent type: catalyst
refractive index
n20/D 1.316 (lit.)
density
1.636 g/mL at 25 °C (lit.)
SMILES string
[H]O[H].[H]O[H].FB(F)F
InChI
1S/BF3.2H2O/c2-1(3)4;;/h;2*1H2
InChI key
MJCYPBSRKLJZTB-UHFFFAOYSA-N
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애플리케이션
Boron trifluoride dihydrate can be used as:
- An activator in Pechmann condensation to synthesize 4-methylcoumarin derivatives by the reaction between substituted phenols and methyl acetoacetate.
- An initiator for the polymerization of benzoxazine.
- A catalyst in the regioselective Fries rearrangement of phenolic esters to give hydroxyphenyl alkyl/aryl ketones.
- A catalyst to prepare 8-hydroxymethyltricyclene acetate by the reaction between camphene and formaldehyde in the presence of methylene chloride-acetic anhydride solvent.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 2 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1A - STOT RE 2 Inhalation - STOT SE 3
표적 기관
Kidney, Respiratory system
Storage Class Code
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
이미 열람한 고객
Cationic polymerization of benzoxazine monomers by boron trifluoride complex.
Polymers & Polymer Composites, 7(6), 409-420 (1999)
Terpene-formaldehyde reactions. II. d-Limonene
The Journal of Organic Chemistry, 33(3), 1156-1159 (1968)
BF3-H2O catalyzed Fries rearrangement of phenolic esters
Catalysis Letters, 114(1), 24-29 (2007)
Pechmann reaction promoted by boron trifluoride dihydrate.
Molecules (Basel), 10(7), 762-766 (2005)
Biochemical pharmacology, 183, 114341-114341 (2020-11-17)
Platelets are the smallest blood cells, and their activation (platelet cohesion or aggregation) at sites of vascular injury is essential for thrombus formation. Since the use of antiplatelet therapy is an unsolved problem, there are now focused and innovative efforts
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