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Merck
CN

438839

1-(苯基磺酰基)吡咯

98%

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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
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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.


pictograms

Exclamation mark

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



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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
438839-5G04061833323281