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Merck
CN

192198

Sigma-Aldrich

2,4,6-三异丙基苯磺酰基肼

90%

别名:

2,4,6-三异丙基苯磺酰基肼, 2,4,6-三异丙基苯磺酰肼, TPSH

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About This Item

线性分子式:
[(CH3)2CH]3C6H2SO2NHNH2
CAS号:
分子量:
298.44
Beilstein:
2145001
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

方案

90%

表单

powder

mp

110-112 °C (dec.) (lit.)

官能团

hydrazine

储存温度

−20°C

SMILES字符串

CC(C)c1cc(C(C)C)c(c(c1)C(C)C)S(=O)(=O)NN

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

InChI key

UGRVYFQFDZRNMQ-UHFFFAOYSA-N

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应用

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.

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)

法规信息

新产品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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访问文档库

2,4,6-Triisopropylbenzenesulfonylhydrazide
Chamberlin AR, et al.
Encyclopedia of Reagents for Organic Synthesis, Second Edition null
Cobalt (II) Porphyrin-Catalyzed Intramolecular Cyclopropanation of N-Alkyl Indoles/Pyrroles with Alkylcarbene: Efficient Synthesis of Polycyclic N-Heterocycles
Reddy AR, et al.
Angewandte Chemie (International ed. in English), 55(5), 1810-1815 (2016)
2, 4, 6-Tri-isopropylbenzenesulphonyl hydrazide: A convenient source of di-imide
Cusack NJ, et al.
Tetrahedron, 32(17) (1976)
Constrained peptides with target-adapted cross-links as inhibitors of a pathogenic protein-protein interaction
Glas A, et al.
Angewandte Chemie (International Edition in English), 53(9), 2489-2493 (2014)
Silver-promoted synthesis of vinyl sulfones from vinyl bromides and sulfonyl hydrazides in water
Zhang G, et al.
Chemical Communications (Cambridge, England), 56(34), 4688-4691 (2020)

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