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Merck
CN

557323

邻甲苯磺酰氯

97%

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线性分子式:
CH3C6H4SO2Cl
化学文摘社编号:
分子量:
190.65
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
205-113-0
MDL number:
Assay:
97%
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InChI key

HDECRAPHCDXMIJ-UHFFFAOYSA-N

InChI

1S/C7H7ClO2S/c1-6-4-2-3-5-7(6)11(8,9)10/h2-5H,1H3

SMILES string

Cc1ccccc1S(Cl)(=O)=O

assay

97%

refractive index

n20/D >1.5580 (lit.)

bp

254 °C (lit.)

density

1.320 g/mL at 25 °C (lit.)

General description

o-Toluenesulfonyl chloride can be synthesized by reacting o-thiocresol in glacial acetic acid with chlorine. It participates in the preparation of 5-chloro-3-phenyl-2,1-benzisoxazole.

Application

o-Toluenesulfonyl chloride may be used in the synthesis of:
  • oxazoline
  • mesityl o-tolyl sulfone
  • allyl o-toluenesulfonate
  • 2-methyl-4′-t-butyldiphenyl sulfone

pictograms

Corrosion

signalword

Danger

hcodes

Hazard Classifications

Skin Corr. 1B

存储类别

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

230.0 °F - closed cup

flash_point_c

110 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

法规信息

危险化学品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Intramolecular nucleophilic participation. V. The role of the ortho-substituent in the solvolysis of o-nitrobenzhydrl bromide and o-nitrobenzyl tosylate.
Mease AD, et al.
Journal of the American Chemical Society, 90(7), 1797-1801 (1968)
Cyclization of Acylaminoalkanols to 2-Oxazolines1.
Boyd RN and Rittner RC.
Journal of the American Chemical Society, 82(8), 2032-2034 (1960)
The Metalation of 4-t-Butyldiphenyl Sulfone with n-Butyllithium1.
Shirley DA and Lehto EA.
Journal of the American Chemical Society, 79(13), 3481-3485 (1957)
Min Wang et al.
Biomaterials, 261, 120301-120301 (2020-09-02)
Local tumor therapy through injectable biodegradable hydrogels with controlled drug release has attracted much attention recently, due to their easy operation, low side effect and efficiency. However, most of the reported therapeutic hydrogel system showed a lack of biodegradation tracking
Rearrangements of sulfones to sulfinic acids via carbanion intermediates.
Truce WE and Brand WW
The Journal of Organic Chemistry, 35(6), 1828-1833 (1970)

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