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Merck
모든 사진(1)

주요 문서

A59506

Sigma-Aldrich

1-Aminoindan

98%

동의어(들):

1-Indanamine

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About This Item

실험식(Hill 표기법):
C9H11N
CAS Number:
Molecular Weight:
133.19
Beilstein:
3196205
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

분석

98%

양식

liquid

refractive index

n20/D 1.561 (lit.)

bp

96-97 °C/8 mmHg (lit.)

mp

15 °C (lit.)

density

1.038 g/mL at 25 °C (lit.)

저장 온도

2-8°C

SMILES string

NC1CCc2ccccc12

InChI

1S/C9H11N/c10-9-6-5-7-3-1-2-4-8(7)9/h1-4,9H,5-6,10H2

InChI key

XJEVHMGJSYVQBQ-UHFFFAOYSA-N

픽토그램

Exclamation mark

신호어

Warning

유해 및 위험 성명서

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

표적 기관

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point (°F)

201.2 °F - closed cup

Flash Point (°C)

94 °C - closed cup

개인 보호 장비

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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문서 라이브러리 방문

이미 열람한 고객

Fumihiko Kitagawa et al.
Analytical sciences : the international journal of the Japan Society for Analytical Chemistry, 21(1), 61-65 (2005-01-29)
Chiral separations of 1-aminoindan (AI) by cyclodextrin electrokinetic chromatography (CDEKC) were investigated on microfluidic quartz chips. By using a microchip electrophoresis (MCE) instrument equipped with a linear-imaging UV detector, the separation process of the enantiomeric compounds was observed. When sulfated
Wilfried Dimpfel et al.
Neuropsychobiology, 62(4), 213-220 (2010-08-18)
Rasagiline and selegiline are classified as monoamine oxidase B (MAO-B) inhibitors. The present investigation deals with time-dependent electrical frequency changes (electropharmacograms) induced by these, as well as by aminoindan, the major metabolite of rasagiline. Adult rats (day-night converted, >5 months
L Zhou et al.
Journal of capillary electrophoresis, 4(6), 279-285 (1998-11-25)
Aminoindanol poses an interesting separation problem because it contains two chiral centers and exists as four stereoisomers. The capillary electrophoretic separation of the cis- and the larger trans-diastereomers of aminoindanol is simply achieved by pH control of the tris buffer
Sofia Glezer et al.
European journal of pharmacology, 472(3), 173-177 (2003-07-23)
The selective monoamine oxidase-B inhibitor selegiline (deprenyl) causes sympathomimetic effects and is metabolised to R(-)-methamphetamine and R(-)-amphetamine. The new monoamine oxidase-B inhibitor rasagiline is devoid of sympathomimetic effects and is metabolised to R(+)-1-aminoindan. Sympathomimetic effects of methamphetamine and 1-aminoindan enantiomers
James M Graham et al.
Bioorganic & medicinal chemistry letters, 18(2), 489-493 (2007-12-28)
As part of an on-going effort to investigate the chemical space requirements for D(2)/5-HT(2A) receptor antagonists as atypical antipsychotics, new 1-aminoindanes were synthesized. The replacement of the heterocycle (oxindole) in ziprasidone with a carbocycle (indane) was well tolerated and was

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