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Merck
CN

539392

2-溴-4′-氰基苯乙酮

96%

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关于此项目

线性分子式:
BrCH2COC6H4CN
化学文摘社编号:
分子量:
224.05
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
96%
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Quality Level

assay

96%

mp

92-96 °C (lit.)

functional group

bromo, ketone, nitrile

SMILES string

BrCC(=O)c1ccc(cc1)C#N

InChI

1S/C9H6BrNO/c10-5-9(12)8-3-1-7(6-11)2-4-8/h1-4H,5H2

InChI key

LJANCPRIUMHGJE-UHFFFAOYSA-N

General description

2-Bromo-4′-cyanoacetophenone can be synthesized from ethylbenzene via aerobic photooxidation using aqueous HBr.

Application

2-Bromo-4′-cyanoacetophenone may be used to synthesize:
  • 3-acylindolizines
  • (2R,3R)-3-[4-(4-cyanophenyl)thiazol-2-yl]-2-(2,4-difluorophenyl)-1-(1H-1,2,4-triazol-1-yl)-2-butanol
  • 1-[2-(4-cyanophenyl)-2-oxoethyl]-1,10-phenanthrolinium bromide


pictograms

CorrosionExclamation mark

signalword

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B

存储类别

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Application of DMF?methyl sulfate adduct in the regioselective synthesis of 3-acylated indolizines.
Przewloka T, et al.
Tetrahedron Letters, 48(33), 5739-5742 (2007)
Synthesis and antifungal activity of novel thiazole-containing triazole antifungals. II. Optically active ER-30346 and its derivatives.
Tsuruoka, Akihiko, et al.
Chemical & Pharmaceutical Bulletin, 46(4), 623-630 (1998)
New 1, 10-phenanthroline derivatives with potential antitumoral activity.
Dumitrascu F, et al.
Rev. Roum. Chim., 53(3), 183-187 (2008)



全球贸易项目编号

货号GTIN
539392-5G04061832100708
539392-25G04061832566634