基本情報
- CAS
39085-59-1- 標準SMILES
CC(C)c1cc(C(C)C)c(S(=O)(=O)NN)c(C(C)C)c1- InChIKey
UGRVYFQFDZRNMQ-UHFFFAOYSA-N- 分子式
- C15H26N2O2S
- 平均分子量
- 298.4 g/mol
- 単同位体質量
- 298.17149907
名称と識別子
- 優先名称
- 2,4,6-Triisopropylbenzenesulphonohydrazide
- IUPAC
- 2,4,6-tri(propan-2-yl)benzenesulfonohydrazide
- 現地名
- 2,4,6-トリイソプロピルベンゼンスルホニルヒドラジド
- 英語名
- 2,4,6-Triisopropylbenzenesulfonyl hydrazide
- 分子式
- C15H26N2O2S
- 分子量
- 298.44
名称と別名
名称をさらに表示
データベース識別子
- CAS
39085-59-1- PubChem CID
- 359333
- DTXSID
DTXSID40192332- ChEMBL
CHEMBL1986656- UNII
- XE77ZV5VCV
- EC Number
- 254-282-7
- Nikkaji
- J261.302F
物性
構造計算による物性
- XLogP
- 3.5
- 極性表面積
- 80.6 Ų
- 水素結合供与体数
- 2
- 水素結合受容体数
- 4
- 回転可能結合数
- 5
- 重原子数
- 20
- 形式電荷
- 0
- 複雑度
- 381
物理化学的性質
- 融点
- 110 · 110-112 °C (dec.) (lit.)
- 沸点
- 396.6 · 396.6±52.0 °C(Predicted)
- 比重(密度)
- 1.075 · 1.075
- 貯蔵温度
- -20 °C · -20°C
- 溶解性
- クロロホルム(微量)、メタノール(微量)
- 酸解離定数(Pka)
- 9.51 · 9.51±0.10(Predicted)
- 外見
- 個体
- 色
- オフホワイト
- 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 データベース
- 39085 · 39085-59-1(CAS DataBase Reference)
化学的性質
化学的特性White crystal
安全と法規制
GHS分類
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.
危険有害性情報
安全データ
- F
- 4.8-10
- wgk
- 3
- ridadr
- UN 1325 4.1/PG III
- hs_code
- 29350090
- 消防法
- 危-5-II
- hazard_code
- Xi
- safety_code
- 22-24/25
- hazard_class
- 4.1
- packing_group
- III
- ストレージクラス
- 11 - Combustible Solids
化学と産業
応用分野
使用2,4,6-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.
調製方法
製造方法2,4,6-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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