192198

2,4,6-Triisopropylbenzenesulfonyl hydrazide

90%

Manufacturer: Sigma Aldrich

CAS Number: 39085-59-1

Synonym(S): 2,4,6-Triisopropylbenzenesulfonohydrazide, TPSH, Trisylhydrazide

Select a Size

Pack Size SKU Availability Price
1 G 192198-1-G In Stock ₹ 13,249.80
5 G 192198-5-G In Stock ₹ 14,213.23

192198 - 1 G

₹ 13,249.80

In Stock

Quantity

1

Base Price: ₹ 13,249.80

GST (18%): ₹ 2,384.964

Total Price: ₹ 15,634.764

Quality Level

100

Assay

90%

form

powder

mp

110-112 °C (dec.) (lit.)

storage temp.

−20°C

SMILES string

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

Other Options

Image Product Name Manufacturer Price Range
50-180-3309
Sigma Aldrich Fine Chemicals Biosciences 2,4,6-Triisopropylbenzenesulfonyl hydrazide 90% | Purity: 90% | Mol Wt: 298.44 | 39085-59-1 | MFCD00014750 | 5G
Sigma Aldrich Fine Chemicals Biosciences ₹ 22,219.93
CS-0068826
2,4,6-Triisopropylbenzenesulfonohydrazide
ChemScene ₹ 2,224.56 - ₹ 10,010.52
AB42689
39085-59-1 | 2,4,6-Triisopropylbenzenesulfonyl hydrazide
A2B Chem ₹ 1,454.52 - ₹ 30,544.92

Description

  • Application: 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.[1]It can be used as a reagent to synthesize: Nitrogen-containing polycyclic compounds by intramolecular cyclopropanation of N-alkyl indoles/pyrroles.[2] Vinyl sulfones by sulfonylation reaction of vinyl bromides.[3] Nitrile derivatives from carbonyl compounds via formation of corresponding hydrazones.[4]

SAFETY INFORMATION

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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−20°C

SMILES string:
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

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UGRVYFQFDZRNMQ-UHFFFAOYSA-N

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