모든 사진(1)
About This Item
실험식(Hill 표기법):
BBr3
CAS Number:
Molecular Weight:
250.52
EC Number:
MDL number:
UNSPSC 코드:
12352101
PubChem Substance ID:
NACRES:
NA.22
추천 제품
vapor density
8.6 (vs air)
Quality Level
vapor pressure
40 mmHg ( 14 °C)
제품 라인
ReagentPlus®
분석
≥99%
색상
colorless to amber
bp
~90 °C (lit.)
mp
−46 °C (lit.)
density
2.60 g/mL at 20 °C (lit.)
SMILES string
BrB(Br)Br
InChI
1S/BBr3/c2-1(3)4
InChI key
ILAHWRKJUDSMFH-UHFFFAOYSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
일반 설명
Boron tribromide is a strong Lewis acid generally employed in the deprotection of -OH and -NH groups. It is a moisture-sensitive liquid, which is also used to cleave esters or ethers into alkyl bromides.
애플리케이션
Reactant for preparation of:
- Drug intermediate 6-nitro-L-DOPA
- Luminescent polystyrene derivatives with sterically protected carbazolylborane moieties
- High-quality boron-doped graphene via Wurtz-type reductive coupling reaction
- Mercapto-(+)-methamphetamine haptens for synthesis of (+)-methamphetamine conjugate vaccines with improved epitope densities
- Micrometer-sized organic molecule-DNA hybrid structures
- Borane complexes via electrophilic aromatic borylation reactions
- A 5-HT2C receptor agonist
- Biphenyl-derivatives possessing tertiary amino groups as β-secretase(BACE1) inhibitors for the treatment of Alzheimer′s disease
- A highly near-IR region fluorescent p-extended boron aza-dipyrromethene moiety unit
- Tetrahydroisoquinoline derivatives via intramolecular cyclization of methoxy-substituted N-phenethylimides
Used to cleave aryl methyl ethers in a synthesis of a benzopyranobenzopyran from a coumarin scaffold.
법적 정보
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Eye Dam. 1 - Skin Corr. 1A
Storage Class Code
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
WGK
WGK 3
개인 보호 장비
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
이미 열람한 고객
Boron Tribromide
Encyclopedia of Reagents for Organic Synthesis, Second Edition (2006)
Boron Halides
Kirk-Othmer Encyclopedia of Chemical Technology (2003)
Qing Zhao et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 203, 472-480 (2018-06-15)
Four homo/heterometallic complexes [Cu3(L)(μ2-OAc)9(CH3OH) 9]·3CHCl3 (1), [Cu2(L)Ca(μ2-NO3)9] (9), [{Cu2(L)Sr(μ2-NO3)9}9]·CH3CH2OH (11) and [Cu2(L)Ba(μ2-OAc)9(OAc)] (14), containing an acyclic naphthalenediol-based ligand H4L, were synthesized and characterized by elemental analyses, IR, UV-Vis, fluorescence spectra, TG-DTA and X-ray crystallography. The complex 1 was obtained by
Tetrahedron Letters, 47, 5909-5909 (2006)
Hui Wang et al.
European journal of medicinal chemistry, 88, 66-73 (2014-09-14)
The pharmacokinetics (PK) and pharmacodynamics (PD) of PT119, a potent Staphylococcus aureus enoyl-ACP reductase (saFabI) inhibitor with a Ki value of 0.01 nM and a residence time of 750 min on the enzyme target, has been evaluated in mice. PT119
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