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Merck
CN

295027

Sigma-Aldrich

三氟化硼

≥99.5%

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About This Item

经验公式(希尔记法):
BF3
CAS号:
分子量:
67.81
EC 号:
MDL编号:
UNSPSC代码:
12352106
PubChem化学物质编号:
NACRES:
NA.22

蒸汽密度

2.38 (21 °C, vs air)

质量水平

方案

≥99.5%

表单

gas

反应适用性

core: boron
reagent type: Lewis acid
reagent type: catalyst
reaction type: Polymerization Reactions

沸点

−100 °C (lit.)

mp

−127 °C (lit.)

SMILES字符串

FB(F)F

InChI

1S/BF3/c2-1(3)4

InChI key

WTEOIRVLGSZEPR-UHFFFAOYSA-N

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警示用语:

Danger

危险声明

危险分类

Acute Tox. 2 Inhalation - Eye Dam. 1 - Press. Gas Compr. Gas - Skin Corr. 1A

补充剂危害

储存分类代码

2A - Gases

WGK

WGK 1

个人防护装备

Faceshields, Gloves, Goggles, multi-purpose combination respirator cartridge (US)

法规信息

新产品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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T Mizuno et al.
The Journal of chemical physics, 136(7), 074305-074305 (2012-03-01)
Recoil frame photoelectron angular distributions (RFPADs) of BF(3) molecules are presented over the energy region of the shape resonance in the F 1s continuum. Time-dependent density functional theory calculations are also given to understand the shape resonance dynamics. The RFPADs
The influence of the acidity of ionic liquids on catalysis.
Xinjiang Cui et al.
ChemSusChem, 3(9), 1043-1047 (2010-08-18)
Ramanathan Rajaganesh et al.
Carbohydrate research, 345(12), 1649-1657 (2010-06-29)
BF(3).Et(2)O-catalysed O-glycosylation of 1,2,3-tri-O-acetyl-4,6-O-butylidene- and ethylidene-beta-d-glucopyranose with different aliphatic and aromatic alcohols proceeds for the most part with complete retention of anomeric configuration. Antioxidant activity of O-glycosides shows significant inhibition (IC(50) approximately 77%). 1,3-Dipolar cycloaddition of terminal alkyne derivatives of
Joseph J Topczewski et al.
The Journal of organic chemistry, 74(18), 6965-6972 (2009-08-25)
The first total synthesis of (+)-schweinfurthin B, a potent and differentially active cytotoxic agent, has been accomplished. Completion of the synthesis required just 16 steps in the longest linear sequence from commercially available vanillin. Key synthetic transformations included a Shi
Diego dos Santos Pisoni et al.
European journal of medicinal chemistry, 45(2), 526-535 (2009-12-04)
This work describes the enantioselective synthesis of a new series of terpenic chiral 9-aminotetrahydroacridine analogues. Several chiral ketones were synthesized from natural monoterpenes in an optically active form and subjected to the cyclodehydration reactions with anthranilonitrile in the presence of

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