323136
Trimethylboroxine
99%
동의어(들):
2,4,6-Trimethyl-1,3,5,2,4,6-trioxatriborinane, 2,4,6-Trimethylboroxine, Methaneboronic anhydride, Trimethyl-1,3,5,2,4,6-trioxatriborinane
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모든 사진(7)
About This Item
실험식(Hill 표기법):
C3H9B3O3
CAS Number:
Molecular Weight:
125.53
Beilstein:
1757008
MDL number:
UNSPSC 코드:
12352103
PubChem Substance ID:
NACRES:
NA.22
추천 제품
Quality Level
분석
99%
양식
liquid
refractive index
n20/D 1.362 (lit.)
bp
78-80 °C (lit.)
mp
−38 °C (lit.)
density
0.898 g/mL at 25 °C (lit.)
SMILES string
Cb1ob(C)ob(C)o1
InChI
1S/C3H9B3O3/c1-4-7-5(2)9-6(3)8-4/h1-3H3
InChI key
GBBSAMQTQCPOBF-UHFFFAOYSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
애플리케이션
Trimethylboroxine (TMB) is a cyclic anhydride of methyl-boronic acid. It can be been used:
- As a derivatizing agent for gas chromatographic/mass spectrometric analysis.
- In the preparation of methylaluminoxane (MAO) which is used in the polymerization of olefins.
- As an electrolyte additive to enhance the interface stability of electrode/electrolyte.
- In methylation of aryl halides by palladium-catalyzed Suzuki-Miyaura coupling reaction.
- In the preparation of CBS (Corey, Bakshi and Shibata) catalysts for asymmetric reductions of ketones to alcohols.
관련 제품
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Flam. Liq. 2 - Skin Corr. 1B
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point (°F)
15.8 °F - closed cup
Flash Point (°C)
-9 °C - closed cup
개인 보호 장비
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
이미 열람한 고객
Tetrahedron Asymmetry, 14, 2115-2118 (2003)
Reactivity of metallocene catalysts for olefin polymerization: influence of activator nature and structure
Pedeutour JN
Macromolecular Rapid Communications, 22(14), 1095-1123 (2001)
Enhanced high voltage performances of layered lithium nickel cobalt manganese oxide cathode by using trimethylboroxine as electrolyte additive
Yu Q, et al.
Electrochimica Acta, 176(14), 919-925 (2015)
Zoltán Dalicsek et al.
Organic letters, 7(15), 3243-3246 (2005-07-16)
[reaction: see text]. An operationally simple and recoverable fluorous CBS methodology was developed. The in situ-generated fluorous oxazaborolidine efficiently catalyzed the reduction of ketones with high enantioselectivity and reactivity. The subsequent recycling of the fluorous prolinol precatalyst was achieved by
Practical methylation of aryl halides by Suzuki-Miyaura coupling.
Gray M, et al.
Tetrahedron Letters, 41(32), 6237-6240 (2000)
Global Trade Item Number
SKU | GTIN |
---|---|
323136-1G | 4061826708354 |
323136-250G | 4061833398319 |
323136-25G | 4061826708361 |
323136-5G | 4061826708378 |
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