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Merck
모든 사진(2)

문서

109223

Sigma-Aldrich

1-Bromoadamantane

99%

동의어(들):

1-Adamantyl bromide

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모든 사진(2)

About This Item

실험식(Hill 표기법):
C10H15Br
CAS Number:
768-90-1
Molecular Weight:
215.13
Beilstein:
1098857
EC Number:
212-200-7
MDL number:
MFCD00074721
UNSPSC 코드:
12352100
PubChem Substance ID:
24846896
NACRES:
NA.22

분석

99%

mp

116-118 °C (lit.)

SMILES string

BrC12C[C@H]3C[C@H](C[C@H](C3)C1)C2

InChI

1S/C10H15Br/c11-10-4-7-1-8(5-10)3-9(2-7)6-10/h7-9H,1-6H2/t7-,8+,9-,10-

InChI key

VQHPRVYDKRESCL-CHIWXEEVSA-N

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일반 설명

1-Bromoadamantane forms inclusion complexes with α-, β-, and γ-cyclodextrins. It causes the alkylation of Co(II) complexes of β-diketones.

애플리케이션

1-Bromoadamantane was used in the synthesis of a new organic–organic nanoscale composite thin-film dielectric.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

Eyeshields, Gloves, type N95 (US)

시험 성적서(COA)

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문서 라이브러리 방문

Jitendra N Tiwari et al.
ChemSusChem, 3(9), 1051-1056 (2010-07-14)
A new organic-organic nanoscale composite thin-film (NCTF) dielectric has been synthesized by solution deposition of 1-bromoadamantane and triblock copolymer (Pluronic P123, BASF, EO20-PO70-EO20), in which the precursor solution has been achieved with organic additives. We have used a sol-gel process
Alkylation of ?-diketones through their co (II), co (III) and zn (II) complexes. 1-Bromoadamantane as alkylating agent.
Gonzalez A, et al.
Tetrahedron Letters, 26(31), 3735-3738 (1985)
P. M. Ivanov et al.
The Journal of organic chemistry, 61(20), 7012-7017 (1996-10-04)
The inclusion complexes between the most commonly used cyclodextrins (alpha-, beta-, and gamma-CD) and 1-bromoadamantane were prepared and studied experimentally by NMR methods and by molecular dynamics simulations (AMBER force field) with solvation. The NMR results suggest host/guest ratios of
Cheng Li et al.
Analytica chimica acta, 1066, 121-130 (2019-04-28)
A visual, rapid, and sensitive method for the detection of two algal metabolites, geosmin (GSM) and 2-methylisoborneol (2-MIB) using a competitive displacement technique based on molecular imprinted polymers (MIPs) and fluorescent tags was developed. In this method, fluorescent tags that

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