Basic information
- 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- Molecular formula
- C15H26N2O2S
- Average molar mass
- 298.4 g/mol
- Monoisotopic mass
- 298.17149907
Names & identifiers
- Preferred name
- 2,4,6-Triisopropylbenzenesulphonohydrazide
- IUPAC
- 2,4,6-tri(propan-2-yl)benzenesulfonohydrazide
- English name
- 2,4,6-Triisopropylbenzenesulfonyl hydrazide
- Molecular formula
- C15H26N2O2S
- Molecular weight
- 298.44
Names & synonyms
Show more names
Database identifiers
- CAS
39085-59-1- PubChem CID
- 359333
- DTXSID
DTXSID40192332- ChEMBL
CHEMBL1986656- UNII
- XE77ZV5VCV
- EC Number
- 254-282-7
- Nikkaji
- J261.302F
Properties
Computed structural properties
- XLogP
- 3.5
- Topological polar surface area
- 80.6 Ų
- Hydrogen bond donors
- 2
- Hydrogen bond acceptors
- 4
- Rotatable bonds
- 5
- Heavy atoms
- 20
- Formal charge
- 0
- Complexity
- 381
Physicochemical properties
- Melting point
- 110 · 110-112 °C (dec.) (lit.)
- Boiling point
- 396.6 · 396.6±52.0 °C(Predicted)
- Density
- 1.075 · 1.075
- storage temp.
- -20 °C · -20°C
- solubility
- Chloroform (Slightly), Methanol (Slightly)
- pka
- 9.51 · 9.51±0.10(Predicted)
- form
- Solid
- color
- Off-White
- Sensitive
- Moisture Sensitive
- 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 DataBase Reference
- 39085 · 39085-59-1(CAS DataBase Reference)
- FDA UNII
- 77 ZV5VCV · XE77ZV5VCV
- UNSPSC Code
- 12352100 · 12352100
- NACRES
- 22 · NA.22
- Symbol(GHS)
- 7 · GHS07
- Signal word
- Warning
- Hazard statements
- 315 · H315-H319-H335
- Precautionary statements
- 261 · P261-P280a-P304+P340-P305+P351+P338-P405-P501a
- PPE
- 95 · Eyeshields, Gloves, type N95 (US)
- Hazard Codes
- Xi
- Safety Statements
- 22 · 22-24/25
- RIDADR
- 1325 · UN 1325 4.1/PG III
- WGK Germany
- 3 · 3
- F
- 4.8 · 4.8-10
- HazardClass
- 4.1 · 4.1
- PackingGroup
- III
- HS Code
- 29350090 · 29350090
- Storage Class
- 11 · 11 - Combustible Solids
Safety & regulation
GHS classification
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.
Hazard information
Safety data
- F
- 4.8-10
- PPE
- Eyeshields, Gloves, type N95 (US)
- wgk
- 3
- ridadr
- UN 1325 4.1/PG III
- hs_code
- 29350090
- Signal word
- Warning
- Symbol(GHS)
- GHS07
- hazard_code
- Xi
- safety_code
- 22-24/25
- hazard_class
- 4.1
- Storage Class
- 11 - Combustible Solids
- packing_group
- III
- Hazard statements
- H315-H319-H335
- Precautionary statements
- P261-P280a-P304+P340-P305+P351+P338-P405-P501a
Chemistry & industry
Applications
UsesAs a reagent for generation of diimide
Uses2,4,6-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.
Preparation methods
Preparation2,4,6-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.
Suppliers100 total
Related reactions
Compound notes
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