2,4,6-Triisopropylbenzenesulphonohydrazide
Grundinformationen
- CAS
39085-59-1- Standard-SMILES
CC(C)c1cc(C(C)C)c(S(=O)(=O)NN)c(C(C)C)c1- InChIKey
UGRVYFQFDZRNMQ-UHFFFAOYSA-N- Summenformel
- C15H26N2O2S
- Durchschnittliche Molmasse
- 298,4 g/mol
- Monoisotopische Masse
- 298,17149907
Namen und Bezeichner
- Bevorzugter Name
- 2,4,6-Triisopropylbenzenesulphonohydrazide
- IUPAC
- 2,4,6-tri(propan-2-yl)benzenesulfonohydrazide
- Englischer Name
- 2,4,6-Triisopropylbenzenesulfonyl hydrazide
- Summenformel
- C15H26N2O2S
- Molmasse
- 298.44
Namen und Synonyme
Weitere Namen anzeigen
Datenbank-Bezeichner
- CAS
39085-59-1- PubChem CID
- 359333
- DTXSID
DTXSID40192332- ChEMBL
CHEMBL1986656- UNII
- XE77ZV5VCV
- EC Number
- 254-282-7
- Nikkaji
- J261.302F
Eigenschaften
Berechnete Struktureigenschaften
- XLogP
- 3,5
- Polarare Oberfläche (TPSA)
- 80,6 Ų
- H-Brücken-Donoren
- 2
- H-Brücken-Akzeptoren
- 4
- Frei drehbare Bindungen
- 5
- Schwere Atome
- 20
- Formalladung
- 0
- Komplexität
- 381
Physikochemische Eigenschaften
- Schmelzpunkt
- 110 · 110-112 °C (dec.) (lit.)
- Siedepunkt
- 396.6 · 396.6±52.0 °C(Predicted)
- Dichte
- 1.075 · 1.075
- storage temp.
- -20 °C · -20°C
- Löslichkeit
- Chloroform (Slightly), Methanol (Slightly)
- pka
- 9.51 · 9.51±0.10(Predicted)
- Aggregatzustand
- Solid
- Farbe
- Off-White
- BRN
- 2145001 · 2145001
- InChI
- InChI=1S/C15H26N2O2S/c1-9(2)12-7-13(10(3)4)15(20(18,19)17-16)14(8-12)11(5)6/h7-11,17H,16H2,1-6H3
- InChIKey
- GBQCDUBJTLROBV-UHFFFAOYSA-N
- SMILES
- C1(S(NN)(=O)=O)=C(C(C)C)C=C(C(C)C)C=C1C(C)C
- CAS Datenbank
- 39085 · 39085-59-1(CAS DataBase Reference)
Sicherheit und Regulatorisches
GHS-Klassifizierung
GHS Classification
Danger
H228 (20%): Flammable solid [Danger Flammable solids]
P210, P240, P241, P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P370+P378, P403+P233, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 5 reports by companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Gefahrenhinweise
Sicherheitsdaten
- F
- 4.8-10
- wgk
- 3
- ridadr
- UN 1325 4.1/PG III
- hs_code
- 29350090
- hazard_code
- Xi
- safety_code
- 22-24/25
- hazard_class
- 4.1
- packing_group
- III
- Speicherklasse
- 11 - Combustible Solids
Chemie und Industrie
Anwendungen
Verwenden2,4,6-Triisopropylbenzenesulfonyl hydrazide (TPSH) is a best source of diazene. It can be used as a selective reducing agent for the reduction of alkenes and other double bonds via in situ formation of diazene (diimide) in the presence of base. TPSH reduction method is efficiently used in the synthesis of polymers and natural products as it tolerates sensitive groups such as esters, ketones, or organometal complexes. It also undergoes condensation reaction with ketones and aldehydes to produce corresponding hydrazones that can be converted into reactive intermediates such as diazoalkanes, carbenes, carbenium ions, and alkyllithiums.It can be used as a reagent to synthesize: Nitrogen-containing polycyclic compounds by intramolecular cyclopropanation of N-alkyl indoles/pyrroles. Vinyl sulfones by sulfonylation reaction of vinyl bromides. Nitrile derivatives from carbonyl compounds via formation of corresponding hydrazones.
Darstellung
synthetische2,4,6-Triisopropylbenzenesulfonyl hydrazide may be prepared in 96% yield by treating commercially available 2,4,6-triisopropylbenzenesulfonyl chloride with hydrazine hydrate in THF, being careful to keep the reaction and workup temperatures below or around 0 °C. The solid can be dried in vacuo over P2O5 for 24 h.
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