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关于此项目
经验公式(希尔记法):
C10H9NO2S
化学文摘社编号:
分子量:
207.25
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
98%
Form:
solid
assay
98%
form
solid
mp
88-91 °C (lit.)
SMILES string
O=S(=O)(c1ccccc1)n2cccc2
InChI
1S/C10H9NO2S/c12-14(13,11-8-4-5-9-11)10-6-2-1-3-7-10/h1-9H
InChI key
PPPXRIUHKCOOMU-UHFFFAOYSA-N
General description
1-(Phenylsulfonyl)pyrrole is a heterocyclic building block. 1-(Phenylsulfonyl) group serves as N-blocking and directing group in various organic syntheses.
Application
1-(Phenylsulfonyl)pyrrole (1-phenylsulfonyl-1H-pyrrole) may be used in the synthesis of 1-(phenylsulfonyl)pyrrole-2-boronic acid, via lithiation of 1-(phenylsulfonyl)-pyrrole. It may be used for the synthesis of 1-phenylsulfonyl-1H-pyrrole-3-sulfonyl chloride derivatives, which affords sulfonamide derivatives by reaction with nitrogen nucleophiles.
signalword
Warning
hcodes
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
Efficient sulfonation of 1-phenylsulfonyl-1H-pyrroles and 1-phenylsulfonyl-1H-indoles using chlorosulfonic acid in acetonitrile.
Janosik T, et al.
Tetrahedron, 62(8), 1669-1707 (2006)
Pyrrole chemistry. XXVIII. Substitution reactions of 1-(phenylsulfonyl) pyrrole and some derivatives.
Anderson HJ, et al.
Canadian Journal of Chemistry, 63(4), 896-902 (1985)
Synthesis of 2-Aryl-1-(phenylsulfonyl) pyrroles.
Grieb JG and Ketcha DM.
Synthetic Communications, 25(14), 2145-2153 (1995)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 438839-5G | 04061833323281 |
