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About This Item
Linear Formula:
CH3C6H4SO2NHNH2
CAS Number:
Molecular Weight:
186.23
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
216-407-3
Beilstein/REAXYS Number:
610130
MDL number:
Assay:
97%
Form:
powder
assay
97%
form
powder
mp
103-108 °C (lit.)
functional group
hydrazine
SMILES string
Cc1ccc(cc1)S(=O)(=O)NN
InChI
1S/C7H10N2O2S/c1-6-2-4-7(5-3-6)12(10,11)9-8/h2-5,9H,8H2,1H3
InChI key
ICGLPKIVTVWCFT-UHFFFAOYSA-N
Related Categories
Application
p-Toluenesulfonyl hydrazide was used as a reagent for the preparation of tosylhydrazones. It was used to prepare dipyrazolo[1,5-a:4′,3′-c]pyridines and 1,2,3-selenadiazole derivatives.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Oral - Aquatic Chronic 2 - Self-react. D
Storage Class
5.2 - Organic peroxides and self-reacting hazardous materials
wgk
WGK 3
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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Mousa Al-Smadi et al.
Molecules (Basel, Switzerland), 13(11), 2740-2749 (2008-11-07)
The commercially available aromatic polyketones 1a-d were utilized for the synthesis of the multi-arm1,2,3-selenadiazole derivatives 3a-d. The preparation starts with the reaction between compounds 1a-d and p-toluenesulfonyl hydrazide to give the corresponding tosylhydrazones 2a-d. Subsequent reaction with selenium dioxide leads
Journal of the American Chemical Society, 114, 966-966 (1992)
Dipyrazolo[1,5-a:4',3'-c]pyridines - a new heterocyclic system accessed via multicomponent reaction.
Wolfgang Holzer et al.
Beilstein journal of organic chemistry, 8, 2223-2229 (2013-02-01)
The synthesis of dipyrazolo[1,5-a:4',3'-c]pyridines is described. Easily obtainable 5-alkynylpyrazole-4-carbaldehydes, p-toluenesulfonyl hydrazide, and an aldehyde or ketone containing an α-hydrogen atom were reacted in a silver triflate catalyzed multicomponent reaction affording new tricyclic compounds with a dipyrazolo[1,5-a:4',3'-c]pyridine core. Detailed NMR spectroscopic
Journal of the American Chemical Society, 115, 2473-2473 (1993)
Anna V Gudmundsdottir et al.
Organic letters, 10(16), 3461-3463 (2008-07-12)
N'-Glycopyranosylsulfonohydrazides are introduced as glycosyl donors for protecting group free synthesis of O-glycosides, glycosyl azides, and oxazolines. Mono- and disaccharides containing a reducing terminal N-acetylglucosamine residue were condensed with p-toluenesulfonylhydrazide to give the desired beta- d-pyranose donors. These donors can
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 14501-1G | 04061838736062 |
| 14502-1G | 04061826652312 |
| 14504-250MG-F | 04061838736086 |
| 14504-1G-F | 04061826652329 |
| 14508-1G | 04061826652336 |
| 14509S-1KG-R | 04061824069440 |
| 752460-1G | 04061832907307 |
| 752452-5G | 04061832907291 |
| 753084-1G | 04061837889585 |
| 14501-250MG | 04061833278727 |
| 14502-250MG | 04061833278734 |
| 14509-1G-F | 04061826652343 |
| P9906-5G | 04061833612903 |
| P9906-1G | 04061838355577 |
| 752444-5G | 04061833600603 |
| 752444-1G | 04061832907277 |
| 752452-1G | 04061832907284 |
| 752460-5G | 04061833600610 |
| 753084-5G | 04061832907543 |
| 132004-100G | 04061838728722 |
| 132004-500G | 04061833544433 |
| 132004-25G | 04061838728739 |
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