CAS 109838-85-9
:(R)-2,5-dihidro-3,6-dimetoxi-2-isopropilpirazina
Descrição:
(R)-2,5-dihidro-3,6-dimetoxi-2-isopropilpirazina é um composto químico caracterizado por sua estrutura única de anel de pirazina, que contribui para suas propriedades aromáticas. Este composto apresenta dois grupos metóxi (-OCH3) nas posições 3 e 6, aumentando sua solubilidade e reatividade. A presença de um grupo isopropílico na posição 2 adiciona ao seu volume estérico, influenciando suas interações e aplicações potenciais. Como uma molécula quiral, ela existe em duas formas enantioméricas, sendo a configuração (R) de particular interesse em vários campos, incluindo a química de sabores e fragrâncias, devido aos seus atributos sensoriais distintos. O composto é tipicamente sintetizado através de reações orgânicas específicas que permitem a introdução seletiva de grupos funcionais. Suas aplicações podem se estender à indústria alimentícia, onde pode ser utilizado como agente aromatizante, bem como no desenvolvimento de fragrâncias. No geral, (R)-2,5-dihidro-3,6-dimetoxi-2-isopropilpirazina é notável por suas características estruturais e potencial utilidade em várias aplicações 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)
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7 produtos.
(R)-3-Isopropyl-2,5-dimethoxy-3,6-dihydropyrazine, 98%
CAS:<p>(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 </p>Fórmula:C9H16N2O2Pureza:98%Cor e Forma:Colorless to yellow to orang, LiquidPeso molecular:184.24(R)-2,5-Dihydro-3,6-dimethoxy-2-isopropylpyrazine
CAS:Fórmula:C9H16N2O2Pureza:96%Cor e Forma:LiquidPeso molecular:184.2355Ref: IN-DA0032ER
1g61,00€5g184,00€10g255,00€1kgA consultar25g509,00€50gA consultar100gA consultar500gA consultar100mg25,00€250mg26,00€(R)-3-Isopropyl-2,5-dimethoxy-3,6-dihydropyrazine
CAS:(R)-3-Isopropyl-2,5-dimethoxy-3,6-dihydropyrazineFórmula:C9H16N2O2Pureza:99%Cor e Forma: colourless to light yellow liquidPeso molecular:184.24g/mol(R)-2-Isopropyl-3,6-dimethoxy-2,5-dihydropyrazine
CAS:Fórmula:C9H16N2O2Pureza:>95.0%(GC)Cor e Forma:Colorless to Yellow clear liquidPeso molecular:184.24(R)-2,5-Dihydro-3,6-dimethoxy-2-isopropylpyrazine
CAS:<p>(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.</p>Fórmula:C9H16N2O2Pureza:Min. 98%Cor e Forma:Colorless Yellow Clear LiquidPeso molecular:184.24 g/mol(R)-2-Isopropyl-3,6-dimethoxy-2,5-dihydropyrazine (>85% Purity)
CAS:Produto Controlado<p>Stability Moisture Sensitive<br>Applications An inhibitor with antitumor activity.<br>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),<br></p>Fórmula:C9H16N2O2Pureza:>85%Cor e Forma:NeatPeso molecular:184.24






