CAS 109838-85-9

(R)-2,5-dihidro-3,6-dimetoxi-2-isopropilpirazina

Descripción:

(R)-2,5-dihidro-3,6-dimetoxi-2-isopropilpirazina es un compuesto químico caracterizado por su estructura única de anillo de pirazina, que contribuye a sus propiedades aromáticas. Este compuesto presenta dos grupos metoxi (-OCH3) en las posiciones 3 y 6, lo que mejora su solubilidad y reactividad. La presencia de un grupo isopropilo en la posición 2 añade a su volumen estérico, influyendo en sus interacciones y aplicaciones potenciales. Como molécula quiral, existe en dos formas enantioméricas, siendo la configuración (R) de particular interés en varios campos, incluida la química de sabores y fragancias, debido a sus atributos sensoriales distintivos. El compuesto se sintetiza típicamente a través de reacciones orgánicas específicas que permiten la introducción selectiva de grupos funcionales. Sus aplicaciones pueden extenderse a la industria alimentaria, donde puede ser utilizado como agente saborizante, así como en el desarrollo de fragancias. En general, (R)-2,5-dihidro-3,6-dimetoxi-2-isopropilpirazina es notable por sus características estructurales y su utilidad potencial en diversas aplicaciones químicas.

Fórmula: C₉H₁₆N₂O₂

InChI: InChI=1/C9H16N2O2/c1-6(2)8-9(13-4)10-5-7(11-8)12-3/h6,8H,5H2,1-4H3/t8-/m1/s1

SMILES: CC(C)[C@@H]1C(=NCC(=N1)OC)OC

Sinónimos:

• (R)-2,5-Dihydro-3,6-dimethoxy-2-isopropylpyrazine
• (R)-2-Isopropyl-3,6-dimethoxy-2,5-dihydropyrazine
• (2R)-3,6-dimethoxy-2-(propan-2-yl)-2,5-dihydropyrazine
• (2R)-2,5-Dihydro-2-isopropyl-3,6-dimethoxypyrazine
• 2,5-Dihydro-3,6-dimethoxy-2-isopropylpyrazine
• (2R)-(-)-2,5-DIHYDRO-3,6-DIMETHOXY-2-ISOPROPYLPYRAZINE
• (2R)-2,5-Dihydro-3,6-dimethoxy-2-(1-methylethyl)pyrazine
• BISLACTIMETHER
• (2R)-(-)-2,5-DIHYDRO-3,6-DIMETHOXY-2-ISOPROPYLPYRAZINE, 98+%
• (2R)-3,6-DIMETHOXY-2-(1-METHYLETHYL)-2,5-DIHYDROPYRAZINE
• (R)-2,5-DIMETHOXY-3-ISOPROPYL-3,6-DIHYDROPYRAZINE
• zR{-2,5-Dihydro-3,6-dimethoxy-2-isopropylpyrazine
• SCHOELLKOPF-HARTWIG-REAGENT
• (2R)-(-)-2,5-Dihydro-3,6-dimethoxy-2-isopropylpyrazine (aka (R )-Schollkopf reagent)
• (R)-2,5-DIHYDRO-3,6-DIMETHOXY-2-ISOPROPYLPIPERAZINE
• (-)-2,5-Dihydro-3,6-dimethoxy-2-isopropylpyrazine
• (R)-Schollkopf Reagent
• Pyrazine, 2,5-dihydro-3,6-dimethoxy-2-(1-methylethyl)-, (2R)-(9CI)

(R)-3-Isopropyl-2,5-dimethoxy-3,6-dihydropyrazine, 98%

CAS: 109838-85-9

(R)-3-Isopropyl-2,5-dimethoxy-3,6-dihydropyrazineChiral auxiliary for the synthesis of -amino acids. It is an inhibitor with antitumor activity. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer

Fórmula: C₉H₁₆N₂O₂

Pureza: 98%

Forma y color: Colorless to yellow to orang, Liquid

Peso molecular: 184.24

Ref: 02-H56077

(R)-2,5-Dihydro-3,6-dimethoxy-2-isopropylpyrazine

CAS: 109838-85-9

Fórmula: C₉H₁₆N₂O₂

Pureza: 96%

Forma y color: Liquid

Peso molecular: 184.2355

Ref: IN-DA0032ER

(R)-3-Isopropyl-2,5-dimethoxy-3,6-dihydropyrazine

CAS: 109838-85-9

(R)-3-Isopropyl-2,5-dimethoxy-3,6-dihydropyrazine

Fórmula: C₉H₁₆N₂O₂

Pureza: 99%

Forma y color: colourless to light yellow liquid

Peso molecular: 184.24g/mol

Ref: 54-OR925455

(R)-2-Isopropyl-3,6-dimethoxy-2,5-dihydropyrazine

CAS: 109838-85-9

Fórmula: C₉H₁₆N₂O₂

Pureza: >95.0%(GC)

Forma y color: Colorless to Yellow clear liquid

Peso molecular: 184.24

Ref: 3B-D3256

(R)-2-Isopropyl-3,6-dimethoxy-2,5-dihydropyrazine

CAS: 109838-85-9

Pureza: 98%

Peso molecular: 184.238998413086

Ref: 10-F790908

(R)-2,5-Dihydro-3,6-dimethoxy-2-isopropylpyrazine

CAS: 109838-85-9

(R)-2,5-Dihydro-3,6-dimethoxy-2-isopropylpyrazine and its enantiomer (S)-2,5-Dihydro-3,6-dimethoxy-2-isopropylpyrazine are also known as Schöllkopf chiral auxiliaries or Schöllkopf reagents, and are used to produce optically pure α-amino acids via asymmetric synthesis. The Schöllkopf reagent can be deprotonated at the prochiral α-carbon, and the resulting enolate is trapped with electrophiles to yield adducts with high (typically > 95% d.e.) diastereoselectivity. The enolate is essentially planar, and the steric bulk of the isopropyl group directs the incoming electrophile to attack from the opposite face, yielding trans adducts. A wide range of electrophiles including alkyl halides, alkyl sulfonates, acyl chlorides, aldehydes, ketones, epoxides, thioketones and enones can be used. Hydrolysis, typically under mild acidic conditions, yields the non-substituted amino acid with high (typically > 95 e.e.) enantiopurity.

Fórmula: C₉H₁₆N₂O₂

Pureza: Min. 98%

Forma y color: Colorless Yellow Clear Liquid

Peso molecular: 184.24 g/mol

Ref: 3D-FD04039

(R)-2-Isopropyl-3,6-dimethoxy-2,5-dihydropyrazine (>85% Purity)

Producto controlado

CAS: 109838-85-9

Stability Moisture Sensitive
Applications An inhibitor with antitumor activity.
References Plumb, J., et al.: Mol. Cancer Ther., 2, 721 (2003), de Ruijter, A., et al.: Biochem. J., 370, 737 (2003), Dey, P., et al.: Curr. Med. Chem., 13, 2909 (2006), Maiso, P., et al.: Cancer Res., 66, 5781 (2006), Paris, M., et al.: J. Med. Chem., 51, 1505 (2008),

Fórmula: C₉H₁₆N₂O₂

Pureza: >85%

Forma y color: Neat

Peso molecular: 184.24

Ref: TR-I824430