CAS 16357-59-8

2-Etoxicarbonil-1-(etoxicarbonil)-1,2-dihidroquinolina

Descripción:

2-Etoxicarbonil-1-(etoxicarbonil)-1,2-dihidroquinolina es un compuesto orgánico caracterizado por su estructura única, que incluye un núcleo de quinolina modificado con grupos funcionales etoxi y etoxicarbonilo. Este compuesto típicamente exhibe propiedades asociadas tanto con sistemas aromáticos como alifáticos, lo que contribuye a su potencial reactividad y solubilidad en varios disolventes orgánicos. La presencia de los grupos etoxi mejora su lipofilia, lo que puede influir en su actividad biológica e interacción con otras moléculas. Además, la estructura de dihidroquinolina sugiere que puede participar en varias reacciones químicas, como oxidación o reducción, debido a la presencia del doble enlace en el sistema de anillo. Este compuesto puede ser de interés en química medicinal, particularmente por sus posibles aplicaciones en el desarrollo de fármacos o como intermediario sintético. Sus características específicas, como el punto de fusión, el punto de ebullición y los datos espectrales, se determinarían típicamente a través de métodos experimentales y pueden variar según la pureza y las condiciones ambientales.

Fórmula: C₁₄H₁₇NO₃

InChI: InChI=1S/C14H17NO3/c1-3-17-13-10-9-11-7-5-6-8-12(11)15(13)14(16)18-4-2/h5-10,13H,3-4H2,1-2H3

Clave InChI: InChIKey=GKQLYSROISKDLL-UHFFFAOYSA-N

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

Sinónimos:

• 1(2H)-Quinolinecarboxylic acid, 2-ethoxy-, ethyl ester
• 1,2-Dihydro-2-ethoxy-1-quinolinecarboxylic acid e
• 1-(Ethoxycarbonyl)-2-ethoxy-1,2-dihydroquinoline
• 2-Ethoxy-1(2H)-quinolinecarboxylic acid ethyl ester
• 2-Ethoxy-1-ethoxycarbonyl-1,2-dihydroquinoline
• 2-Ethoxy-N-(ethoxycarbonyl)-1,2-dihydroquinoline
• EEDQ~N-Ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline
• Ethyl 1,2-dihydro-2-ethoxy-1-quinolinecarboxylate
• Ethyl 2-ethoxy-1(2H)-quinolinecarboxylate
• N-Carbethoxy-2-ethoxy-1,2-dihydroquinoline
• N-Ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline
• NSC 147831
• ethyl (2R)-2-ethoxyquinoline-1(2H)-carboxylate
• ethyl (2S)-2-ethoxyquinoline-1(2H)-carboxylate
• ethyl 2-ethoxyquinoline-1(2H)-carboxylate
• ethyl N-(2-ethoxy-1,2-dihydroquinoline)carboxylate

1-Ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline

CAS: 16357-59-8

Fórmula: C₁₄H₁₇NO₃

Pureza: >98.0%(T)(HPLC)

Forma y color: White to Light yellow to Light orange powder to crystal

Peso molecular: 247.29

Ref: 3B-E0363

2-Ethoxy-1-ethoxycarbonyl-1,2-dihydroquinoline, 99%

CAS: 16357-59-8

2-Ethoxy-1-ethoxycarbonyl-1,2-dihydroquinoline is an irreversible membrane-bound receptor antagonist. It is used in synthetic chemistry, discovery, process RD. It also acts as coupling reagents.This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. So

Fórmula: C₁₄H₁₇NO₃

Pureza: 99%

Forma y color: Crystals or powder or crystalline powder, White to cream

Peso molecular: 247.29

Ref: 02-A13724

EEDQ

CAS: 16357-59-8

EEDQ permits the coupling of acylamino acids with amino acid esters in high yield without concomitant racemization. In a study aiming at the optimization of the coupling of 3,5-dinitrobenzoyl-Leu to 3-aminopropyl-silica (Yang et al.) significant levels of racemization were observed with all the tested coupling reagents except for EEDQ .

Fórmula: C₁₄H₁₇NO₃

Pureza: > 99%

Forma y color: Light Beige Powder

Peso molecular: 247.29

Ref: 01-4015690

1(2H)-Quinolinecarboxylic acid, 2-ethoxy-, ethyl ester

CAS: 16357-59-8

Fórmula: C₁₄H₁₇NO₃

Pureza: 95%

Forma y color: Solid

Peso molecular: 247.2897

Ref: IN-DA001U8Q

Ethyl 1,2-dihydro-2-ethoxyquinoline-1-carboxylate

CAS: 16357-59-8

Ethyl 1,2-dihydro-2-ethoxyquinoline-1-carboxylate

Fórmula: C₁₄H₁₇NO₃

Pureza: 99%

Forma y color: off white crystalline solid

Peso molecular: 247.29g/mol

Ref: 54-OR61179

2-Ethoxy-1-ethoxycarbonyl-1,2-dihydroquinoline

CAS: 16357-59-8

Fórmula: C₁₄H₁₇NO₃

Peso molecular: 247.29

Ref: 7W-GM0340

2-Ethoxy-1-ethoxycarbonyl-1,2-dihydroquinoline

CAS: 16357-59-8

2-Ethoxy-1-ethoxycarbonyl-1,2-dihydroquinolin, also known as EEDQ, is a peptide coupling reagent used to couple acyl amino acids to amino acid esters. EEDQ can be used in a one-step procedure in solution and solid-phase synthesis, achieving good yields with suppression of racemisation. EEDQ is used in the formation of antibody-drug conjugates and DNA-encoded bioconjugates formed from the reaction of an amine, a carboxylic acid and a DNA fragment. EEDQ is also an irreversible dopamine-receptor antagonist (see N-Ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline for Pharmaceutical and Diagnostic Industries).

Fórmula: C₁₄H₁₇NO₃

Pureza: Min. 98 Area-%

Forma y color: White Powder

Peso molecular: 247.29 g/mol

Ref: 3D-FE40640

N-Ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline

CAS: 16357-59-8

Fórmula: C₁₄H₁₇NO₃

Pureza: 95%

Forma y color: Solid, Powder or Crystalline Powder or Granules or Chunks

Peso molecular: 247.294

Ref: 10-F003625

EEDQ extrapure, 99%

CAS: 16357-59-8

Fórmula: C₁₄H₁₇NO₃

Pureza: min. 99%

Forma y color: White to off-white, Crystalline powder

Peso molecular: 247.30

Ref: SR-62813

2-Ethoxy-1-ethoxycarbonyl-1,2-dihydroquinoline

Producto controlado

CAS: 16357-59-8

Applications 2-Ethoxy-1-ethoxycarbonyl-1,2-dihydroquinoline is used in the synthesis of Glycochenodeoxycholic Acid 3-Sulfate Disodium Salt which is a bile salt formed in the liver from chenodeoxycholate and glycine, usually as the sodium salt. It acts as a detergent to solubilize fats for absorption and is itself absorbed. It is a cholagogue and choleretic.
References Parmentier, G. , et al.: Steroids, 30, 583 (1977), Tserng, K.Y., et al.: Lipids, 13, 479 (1978),

Fórmula: C₁₄H₁₇NO₃

Forma y color: Neat

Peso molecular: 247.29

Ref: TR-E891880

N-Ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline

CAS: 16357-59-8

N-Ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline is a transcriptional regulator that is structurally related to the 2-adrenergic receptor agonist, clonidine. It binds to the 5HT2 receptor and has been shown to have antimicrobial properties. N-Ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline has been shown to inhibit viral resistance in animals infected with influenza A virus. This drug also inhibits prolactin release in rats and humans through its binding to dopamine receptors. NEDQ is an inhibitor of human serum prolactin release.

Fórmula: C₁₄H₁₇NO₃

Pureza: Min. 99.0 Area-%

Peso molecular: 247.30 g/mol

Ref: 3D-E-5001

EEDQ

CAS: 16357-59-8

EEDQ: irreversible dopamine antagonist; specifically reacts with carboxyl groups, couples acylamino acids without racemization.

Fórmula: C₁₄H₁₇NO₃

Forma y color: Solid

Peso molecular: 247.29

Ref: TM-T71923