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Merck
모든 사진(2)

주요 문서

B79803

Sigma-Aldrich

3-Bromopropylamine hydrobromide

98%

동의어(들):

3-Aminopropyl bromide hydrobromide

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About This Item

Linear Formula:
BrCH2CH2CH2NH2 · HBr
CAS Number:
Molecular Weight:
218.92
Beilstein:
3906418
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

분석

98%

양식

crystals

mp

171-172 °C (lit.)

SMILES string

Br.NCCCBr

InChI

1S/C3H8BrN.BrH/c4-2-1-3-5;/h1-3,5H2;1H

InChI key

PQIYSSSTRHVOBW-UHFFFAOYSA-N

유사한 제품을 찾으십니까? 방문 제품 비교 안내

애플리케이션

3-Bromopropylamine hydrobromide is commonly used as a reagent to introduce propylamine group to the molecular skeleton. Some of the other reported applications include:
  • Synthesis of photochemically and thermally reactive azobenzene rotaxane and indolocarbazole-containing [2]rotaxane.
  • Synthesis of indenoisoquinoline based active topoisomerase I inhibitors as anticancer agents.

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

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

dust mask type N95 (US), Eyeshields, Gloves


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시험 성적서(COA)

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문서 라이브러리 방문

이미 열람한 고객

Interlocked host anion recognition by an indolocarbazole-containing [2] rotaxane.
Brown A, et al.
Journal of the American Chemical Society, 131(13), 4937-4952 (2009)
Maya Juenet et al.
Biomaterials, 156, 204-216 (2017-12-08)
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Optimization of the indenone ring of indenoisoquinoline topoisomerase I inhibitors.
Morrell A, et al.
Journal of Medicinal Chemistry, 50(18), 4388-4404 (2007)
Antagonist analogue of 6-[3 `-(1-adamantyl)-4 `-hydroxyphenyl]-2-naphthalenecarboxylic acid (AHPN) family of apoptosis inducers that effectively blocks AHPN-induced apoptosis but not cell-cycle arrest.
Dawson M I, et al.
Journal of Medicinal Chemistry, 47(14), 3518-3536 (2004)
Synthesis and anticancer activity of simplified indenoisoquinoline topoisomerase I inhibitors lacking substituents on the aromatic rings.
Nagarajan M, et al.
Journal of Medicinal Chemistry, 47(23), 5651-5661 (2004)

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