CAS 111969-64-3
:(1R,2S,5R)-5-Metil-2-(1-metiletil) ciclohexil 2,2-dihidroxiacetato
Descripción:
(1R,2S,5R)-5-Metil-2-(1-metiletil) ciclohexil 2,2-dihidroxiacetato, con número CAS 111969-64-3, es un compuesto químico caracterizado por su estereoequilibrio específico y grupos funcionales. Esta sustancia presenta un anillo de ciclohexano sustituido con un grupo metilo y un grupo isopropilo, lo que contribuye a sus características hidrofóbicas. La presencia del moiety 2,2-dihidroxiacetato introduce grupos hidroxilo, que pueden mejorar su solubilidad en disolventes polares y pueden influir en su reactividad e interacciones con sistemas biológicos. La configuración estereoquímica indica que tiene centros quirales, lo que puede afectar sus propiedades farmacológicas y actividad biológica. Tales compuestos son a menudo estudiados por sus posibles aplicaciones en productos farmacéuticos, agroquímicos o como intermediarios en la síntesis orgánica. Comprender sus propiedades físicas, como el punto de fusión, el punto de ebullición y la solubilidad, así como su reactividad con otras especies químicas, es crucial para su aplicación en diversos campos.
Fórmula:C12H22O4
InChI:InChI=1S/C12H22O4/c1-7(2)9-5-4-8(3)6-10(9)16-12(15)11(13)14/h7-11,13-14H,4-6H2,1-3H3/t8-,9+,10-/m1/s1
Clave InChI:InChIKey=BWZMJRSMHQDFIT-KXUCPTDWSA-N
SMILES:O(C(C(O)O)=O)[C@H]1[C@H](C(C)C)CC[C@@H](C)C1
Sinónimos:- (1R,2S,5R)-5-Methyl-2-(1-Methylethyl)Cyclohexyl Dihydroxy-Acetate
- (1R,2S,5R)-5-Methyl-2-(1-methylethyl)cyclohexyl 2,2-dihydroxyacetate
- (1S,2R,5S)-5-methyl-2-(1-methylethyl)cyclohexyl dihydroxyacetate
- 2,2-Dihydroxyacetic Acid (-)-Menthyl Ester
- Acetic acid, 2,2-dihydroxy-, (1R,2S,5R)-5-methyl-2-(1-methylethyl)cyclohexyl ester
- Acetic acid, dihydroxy-, (1R,2S,5R)-5-methyl-2-(1-methylethyl)cyclohexyl ester
- Acetic acid, dihydroxy-, 5-methyl-2-(1-methylethyl)cyclohexyl ester, [1R-(1α,2β,5α)]-
- Glyoxylic acid (1S)-menthyl ester hydrate
- L-Menthyl glyoxylate hydrate
- L-Mgh
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Encontrado 8 productos.
(1R,2S,5R)-2-Isopropyl-5-methylcyclohexyl 2,2-Dihydroxyacetate
CAS:Fórmula:C12H22O4Pureza:>98.0%(GC)Forma y color:White to Almost white powder to crystalPeso molecular:230.30(1R)-(-)-Menthyl glyoxylate monohydrate, 98%
CAS:<p>This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci</p>Fórmula:C12H22O4Pureza:98%Forma y color:White to cream, powderPeso molecular:230.30(1R,2S,5R)-2-Isopropyl-5-methylcyclohexyl 2,2-dihydroxyacetate
CAS:Fórmula:C12H22O4Pureza:97%Forma y color:SolidPeso molecular:230.3007(1R,2S,5R)-2-Isopropyl-5-methylcyclohexyl 2,2-dihydroxyacetate
CAS:<p>(1R,2S,5R)-2-Isopropyl-5-methylcyclohexyl 2,2-dihydroxyacetate</p>Pureza:98%Forma y color:White PowderPeso molecular:230.30068g/mol(1R,2S,5R)-2-Isopropyl-5-methylcyclohexyl 2,2-dihydroxyacetate
CAS:Fórmula:C12H22O4Pureza:97%Forma y color:SolidPeso molecular:230.304L-Menthyl 2,2-Dihydroxyacetate
CAS:Producto controlado<p>Applications L-Menthyl 2,2-Dihydroxyacetate is used as a reagent in the synthesis of Lamivudine (L172500); a potent nucleoside reverse transcriptase inhibitor used for the treatment of chronic hepatitis B. L-Menthyl 2,2-Dihydroxyacetate is also used as a reagent in the synthesis of 4-acetoxy-3-hydroxyethylazetidin-2-one, a key intermediate for the preparation of penem and carbapenem antibiotics.<br>References Morris, D.M., J. Pharm. Biomed. Anal., 12, 255 (1944); Nevens, B.F., et al.: Gastroenterology, 113, 1258 (1997); Perry, C.M., et al.: Drugs, 53, 657 (1977); Goodyear, M.D., et al.: Tetrahedron Lett., 46, 8535 (2005); Kametani, T., et al.: Heterocycles, 25, 241 (1987)<br></p>Fórmula:C12H22O4Forma y color:NeatPeso molecular:230.3L-Menthyl 2,2-dihydroxyacetate
CAS:<p>L-Menthyl 2,2-dihydroxyacetate is a synthetic compound that belongs to the group of salicylic acid derivatives. It is an intermediate in the synthesis of other compounds and can be recycled. L-Menthyl 2,2-dihydroxyacetate reacts with primary amines to form iminoacetic esters and glyoxylates by acidic hydrolysis. The reaction time depends on the type of amine and the acidity of the solution. This compound has been used as a reagent to synthesize maleic anhydride from maleic acid. L-Menthyl 2,2-dihydroxyacetate is also used in methodologies for oxidizing aromatic compounds to produce benzoic acids or phenols.</p>Fórmula:C12H22O4Pureza:Min. 95%Forma y color:PowderPeso molecular:230.3 g/mol







