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Merck
CN

697893

6-溴喹啉

97%

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关于此项目

经验公式(希尔记法):
C9H6BrN
化学文摘社编号:
分子量:
208.05
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
226-238-7
MDL number:
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产品名称

6-溴喹啉, 97%

InChI key

IFIHYLCUKYCKRH-UHFFFAOYSA-N

InChI

1S/C9H6BrN/c10-8-3-4-9-7(6-8)2-1-5-11-9/h1-6H

SMILES string

Brc1ccc2ncccc2c1

assay

97%

form

solid

refractive index

n20/D 1.663

density

1.538 g/mL at 25 °C

functional group

bromo

pictograms

CorrosionExclamation mark

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

>230.0 °F

flash_point_c

> 110 °C

ppe

dust mask type N95 (US), Eyeshields, Gloves

法规信息

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历史批次信息供参考:

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Lot/Batch Number

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Alexander V Shaferov et al.
Sensors (Basel, Switzerland), 20(11) (2020-06-11)
Pd(0)-catalyzed amination was employed for the synthesis of a new family of (S)-1,1'-bianaphthalene-2,2'-diamine derivatives possessing additional chiral and fluorophore substituents. The compounds thus obtained were tested as potential detectors of seven amino alcohols, and some of them were found to
Oleg V Larionov et al.
Organic letters, 16(3), 864-867 (2014-01-15)
A one-step transformation of heterocyclic N-oxides to 2-alkyl-, aryl-, and alkenyl-substituted N-heterocycles is described. The success of this broad-scope methodology hinges on the combination of copper catalysis and activation by lithium fluoride or magnesium chloride. The utility of this method

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