CAS 38428-14-7

2-Methylpropyl 2-(2-methylpropoxy)-1(2H)-quinolinecarboxylate

Description:

2-Methylpropyl 2-(2-methylpropoxy)-1(2H)-quinolinecarboxylate, with the CAS number 38428-14-7, is an organic compound characterized by its complex structure, which includes a quinoline ring system. This compound features a carboxylate functional group, indicating it is an ester, and it is substituted with a 2-methylpropyl group and a 2-methylpropoxy group. The presence of these alkyl groups contributes to its hydrophobic nature, potentially influencing its solubility in organic solvents rather than water. The quinoline moiety is known for its biological activity, often exhibiting properties such as antimicrobial or antitumor effects. The compound's molecular structure suggests it may participate in various chemical reactions typical of esters, including hydrolysis and transesterification. Its specific applications and reactivity would depend on the context of its use, particularly in pharmaceuticals or agrochemicals, where quinoline derivatives are often explored for their therapeutic potential. Safety and handling precautions should be observed, as with all chemical substances, due to potential toxicity or reactivity.

Formula: C₁₈H₂₅NO₃

InChI: InChI=1S/C18H25NO3/c1-13(2)11-21-17-10-9-15-7-5-6-8-16(15)19(17)18(20)22-12-14(3)4/h5-10,13-14,17H,11-12H2,1-4H3

InChI key: InChIKey=LPBHYOYZZIFCQT-UHFFFAOYSA-N

SMILES: C(OCC(C)C)(=O)N1C=2C(C=CC1OCC(C)C)=CC=CC2

Synonyms:

• 1(2H)-Quinolinecarboxylic acid, 2-(2-methylpropoxy)-, 2-methylpropyl ester
• 1-Isobutoxycarbonyl-2-isobutoxy-1,2-dihydroquinoline
• 2-Isobutoxy-1-isobutoxycarbonyl-1,2-dihydroquinoline
• 2-Isopropoxy-1-isopropoxycarbonyl-1,2-dihydroquinoline
• 2-Methylpropyl 2-(2-methylpropoxy)-1(2H)-quinolinecarboxylate
• 2-Methylpropyl 2-(2-methylpropoxy)-1,2-dihydroquinoline-1-carboxylate
• 2-methylpropyl (2R)-2-(2-methylpropoxy)quinoline-1(2H)-carboxylate
• 2-methylpropyl (2S)-2-(2-methylpropoxy)quinoline-1(2H)-carboxylate
• 2-methylpropyl 2-(2-methylpropoxy)quinoline-1(2H)-carboxylate
• Iidq (2-Isobutoxy-1-Isobutoxycarbonyl-1,2-Dihydro
• Iidq 1-Isobutoxycarbonyl-2-Isobutoxy-1,2-Dihydroquinoline
• Isobutyl 1,2-dihydro-2-isobutoxy-1-quinoline-carboxylate
• NSC 332545

Isobutyl 1,2-dihydro-2-isobutoxy-1-quinoline-carboxylate

CAS: 38428-14-7

Formula: C₁₈H₂₅NO₃

Purity: 95%

Color and Shape: Liquid

Molecular weight: 303.3960

Ref: IN-DA00351L

Isobutyl 2-Isobutoxyquinoline-1(2H)-Carboxylate

CAS: 38428-14-7

Isobutyl 2-Isobutoxyquinoline-1(2H)-Carboxylate

Purity: 95%

Molecular weight: 303.40g/mol

Ref: 54-OR1013583

1-Isobutoxycarbonyl-2-isobutoxy-1,2-dihydroquinoline

CAS: 38428-14-7

Formula: C₁₈H₂₅NO₃

Purity: 95%

Color and Shape: Liquid, Clear

Molecular weight: 303.402

Ref: 10-F033672

2-Isobutoxy-1-isobutoxycarbonyl-1,2-dihydroquinoline

CAS: 38428-14-7

2-Isobutoxy-1-isobutoxycarbonyl-1,2-dihydroquinoline, also known as IIDQ, is an amide coupling reagent utilised in liquid-phase synthesis. With IIDQ there is no need for the pre-activation step and the efficiency of the coupling is not influenced by the order of the addition of the reagents (amine, carboxylic acid, IIDQ). Furthermore, no guanidinium species are formed with IIDQ, and IIDQ is stable in presence of base. IIDQ is mainly applied in its polymer-supported form, polystyrene-supported IIDQ (PS-IIDQ), which is stable, reactive and efficient. PS-IIDQ requires a simpler purification compared to the free IIDQ and can be easily regenerated. Some applications of PS-IIDQ are in the synthesis of protein conjugates for antibody development and xanthine derivatives to be used as adenosine receptor antagonists.

Formula: C₁₈H₂₅NO₃

Purity: Min. 95%

Color and Shape: Colourless to light yellow viscous clear liquid.

Molecular weight: 303.4 g/mol

Ref: 3D-FI33684