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116173

2-溴-3-吡啶醇

99%

别名:

2-溴-3-羟基吡啶

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关于此项目

经验公式（希尔记法）:
C5H4BrNO
化学文摘社编号:
6602-32-0
分子量:
174.00
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24847268
EC Number:
229-547-5
Beilstein/REAXYS Number:
109829
MDL number:
MFCD00006220
Assay:
99%
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Quality Level

100

assay

99%

mp

185-188 °C (lit.)

functional group

bromo

SMILES string

Oc1cccnc1Br

InChI

1S/C5H4BrNO/c6-5-4(8)2-1-3-7-5/h1-3,8H

InChI key

YKHQFTANTNMYPP-UHFFFAOYSA-N

Application

2-Bromo-3-pyridinol has been used in the preparation of 2-bromo-4,6-diiodo-3-pyridinol. It has also been used in the total synthesis of pterocellin A by reacting with kojic acid.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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:

分析证书(COA)

Lot/Batch Number
STBF8422V
STBC2640V
08112MH
S44277
00910JH

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Halogenation of Pyridinols using Bis(sym-collidine)iodine(I) and Bis(sym-collidine)bromine(I) hexafluorophosphate.
Tetrahedron Letters, 38(14), 2467-2470 (1997)
Meaghan M O'Malley et al.
Organic letters, 8(12), 2651-2652 (2006-06-02)
The first total synthesis of pterocellin A (1) was achieved in 10 linear steps from commercially available kojic acid (6) and 2-bromo-3-pyridinol (11) in a convergent sequence. The key constructive steps are a directed lithiation to couple two pyridines and

全球贸易项目编号

货号GTIN
116173-5G04061832241739
116173-25G04061832241722