CAS 39217-91-9

Quinoline,1,2,3,4-tetrahydro-5-nitro-

Description:

Quinoline, 1,2,3,4-tetrahydro-5-nitro- is a nitrogen-containing heterocyclic compound characterized by its fused ring structure, which includes a quinoline framework. This compound features a tetrahydro configuration, indicating that it has undergone partial hydrogenation, resulting in a saturated form of the quinoline ring. The presence of a nitro group (-NO2) at the 5-position contributes to its chemical reactivity and potential applications in various fields, including pharmaceuticals and agrochemicals. The nitro group can influence the compound's electronic properties, making it a candidate for further chemical modifications. Typically, such compounds exhibit biological activity, which may include antimicrobial or antitumor properties, although specific biological effects would depend on the context of use and further studies. Quinoline derivatives are often explored for their roles in medicinal chemistry due to their structural diversity and ability to interact with biological targets. Safety and handling precautions should be observed, as with many nitro compounds, due to potential toxicity and environmental concerns.

Formula: C₉H₁₀N₂O₂

Synonyms:

• 5-Nitro-1,2,3,4-Tetrahydro-Quinoline Hydrochloride

Quinoline, 1,​2,​3,​4-​tetrahydro-​5-​nitro-

CAS: 39217-91-9

Formula: C₉H₁₀N₂O₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 178.1879

Ref: IN-DA0075ZH

5-Nitro-1,2,3,4-tetrahydroquinoline

CAS: 39217-91-9

5-Nitro-1,2,3,4-tetrahydroquinoline

Purity: 97%

Molecular weight: 178.19g/mol

Ref: 54-OR85714

5-NITRO-1,2,3,4-TETRAHYDROQUINOLINE

CAS: 39217-91-9

Formula: C₉H₁₀N₂O₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 178.191

Ref: 10-F301769

5-Nitro-1,2,3,4-tetrahydroquinoline

CAS: 39217-91-9

5-Nitro-1,2,3,4-tetrahydroquinoline is an amine that is used in the synthesis of other chemicals. It is selective for transfer reactions because it can transfer to sulfate. The reaction selectivity is determined by the module and the reaction solution. The efficiency of the carbenium ion can be increased by adjusting the pH to make it more acidic. 5-Nitro-1,2,3,4-tetrahydroquinoline has a high yield and can be synthesized with a high degree of purity by using ammonium sulfate as a transfer agent in a neutral solution.

Formula: C₉H₁₀N₂O₂

Purity: Min. 95%

Molecular weight: 178.19 g/mol

Ref: 3D-PBA21791