24 Results for "

chiral intermediate

" in MedChemExpress (MCE) Product Catalog:
Products (24)

24 Results for "chiral intermediate" in MCE Product Catalog:

Cat. No.: HY-Y1131
CAS No.: 24915-95-5
Synonyms: Ethyl (R)-3-hydroxybutanoate
Ethyl (R)-3-hydroxybutyrate is an organic compound commonly used as a starting material for chiral chemical synthesis. It can be used in the preparation of medicines, spices, fine chemicals and food additives, etc., and is widely used in medicine, cosmetics and food industries. In addition, this compound is also used as a substrate or intermediate in some biochemical reactions
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Cat. No.: HY-40228
CAS No.: 196929-78-9
Synonyms: (R)-2-Methylpropane-2-sulfinamide
(R)-(+)-tert-Butylsulfinamide ((R)-2-Methylpropane-2-sulfinamide) is a chiral reagent commonly used in the asymmetric synthesis of compounds such as amines, amino acids, and amino alcohols. (R)-(+)-tert-Butylsulfinamide achieves stereoselective reactions by condensing with carbonyl groups to form sulfinyl imine intermediates, and after the reaction, this group can be removed under acidic conditions to obtain the target product .
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Cat. No.: HY-69348
CAS No.: 102308-32-7
(S)-(-)-3-Boc-2,2-dimethyloxazolidine-4-carboxaldehyde is a chiral compound. (S)-(-)-3-Boc-2,2-dimethyloxazolidine-4-carboxaldehyde is commonly used as a chiral intermediate in asymmetric synthesis and has important applications in the field of organic synthesis .
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Cat. No.: HY-76476
CAS No.: 86087-23-2
Synonyms: (+)-3-Hydroxytetrahydrofuran
Research Areas:  

Others

(S)-Tetrahydrofuran-3-ol ((+)-3-Hydroxytetrahydrofuran) is a secondary alcohol and the (S)-enantiomer of Tetrahydrofuran-3-ol. (S)-Tetrahydrofuran-3-ol serves as a crucial chiral alcohol intermediate for the human immunodeficiency virus inhibitor Amprenavir (HY-17430). (S)-Tetrahydrofuran-3-ol is applicable to researches on chiral biocatalysis and synthesis of HIV protease inhibitor intermediates .
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Cat. No.: HY-W016042
CAS No.: 13504-85-3
N-Cbz-Hydroxy-L-proline is a chiral N-Cbz-protected amino acid derivative. N-Cbz-Hydroxy-L-proline is commonly used in the synthesis of polypeptides and pharmaceutical intermediates. N-Cbz-Hydroxy-L-proline undergoes decarboxylation under AlCl3/HFIP conditions .
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Cat. No.: HY-I0169
CAS No.: 196601-69-1
Target:  

Drug Metabolite

Research Areas:  

Neurological Disease

(R)-Amino-N-benzyl-3-methoxypropionamide is a key intermediate for the synthesis of the antiepileptic agent (R)-Lacosamide. To improve its chiral purity and chemical stability, (R)-Amino-N-benzyl-3-methoxypropionamide can react with phosphoric acid to form a phosphate salt. Detected by high performance liquid chromatography (HPLC), this phosphate salt exhibits extremely high chiral purity, with the content of the R-enantiomer reaching up to 99.37% .
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Cat. No.: HY-W012846A
CAS No.: 2319-57-5
Synonyms: L-1,2,3,4-Butanetetrol
L-Threitol (L-1,2,3,4-Butanetetrol) is a four-carbon sugar alcohol. L-Threitol serves as an important pharmaceutical intermediate and can be used in the synthesis of other active compounds, such as anticancer agents and chiral compounds .
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Cat. No.: HY-W001294
CAS No.: 109431-87-0
(R)-(-)-N-Boc-3-pyrrolidinol is a chiral pyrrolidine derivative. After undergoing configuration inversion via the Mitsunobu reaction, (R)-(-)-N-Boc-3-pyrrolidinol can serve as a precursor for the (3S)-aryloxypyrrolidine fragment, which is used to construct key intermediates of FXa inhibitors (such as DX-9065a (HY-10722)) and various chiral drugs. (R)-(-)-N-Boc-3-pyrrolidinol can be applied in studies related to arrhythmia .
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Cat. No.: HY-W002041
CAS No.: 13325-10-5
Synonyms: 4-Amino-1-butanol
Research Areas:  

Others

4-Aminobutan-1-ol (4-Amino-1-butanol) is a linear γ-amino alcohol bearing both a primary amino group and a primary hydroxyl group, which serves as a starting material for the synthesis of pyridine-based Schiff bases. As an important intermediate, 4-Aminobutan-1-ol can be used in the synthesis of GABA derivatives, chiral ligands and other active compounds .
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Cat. No.: HY-79334
CAS No.: 4254-15-3
(S)-(+)-1,2-Propanediol is an endogenous metabolite. (S)-(+)-1,2-Propanediol can be used as an organic solvent and diluent in drug preparations. (S)-(+)-1,2-Propanediol can also be used as a chiral synthetic intermediate and a substrate for enzyme research .
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Cat. No.: HY-32959
CAS No.: 135884-31-0
N-Boc-2-pyrroleboronic acid is an organic synthesis intermediate used primarily in the synthesis of chiral pharmaceutical molecules and biologically active molecules. The boronic acid on the pyrrole ring can participate in Suzuki coupling reactions. The boronic acid can be oxidized to a hydroxyl group under the action of nitrogen oxides, and after tautomerization, it can be further transformed into 2-oxo-2,5-dihydro-1-pyrrolecarboxylic acid tert-butyl ester .
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Cat. No.: HY-W142618
CAS No.: 13265-84-4
D-Glucal is an organic compound belonging to the family of aldoses, which are monosaccharides containing an aldehyde functional group. It has a six-carbon structure and is derived from glucose by oxidation of the primary alcohol group at carbon 1 to an aldehyde group. D-Glucal is a white crystalline solid that is soluble in water and has a sweet taste. It is an important intermediate in the chemical synthesis of a wide variety of compounds, including pharmaceuticals, agrochemicals, and natural products. D-Glucal can be converted into other carbohydrate derivatives such as glycosides, glycoconjugates and amino sugars. It also plays a role in the study of carbohydrate chemistry, where it is used as a chiral building block for the synthesis of complex structures.
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Cat. No.: HY-W012618
CAS No.: 93-54-9
Target:  

Drug Intermediate

Research Areas:  

Others

1-Phenyl-1-propanol is an isomer of phenylpropanol. 1-Phenyl-1-propanol can serve as a fragrance or flavor enhancer, and as a chiral intermediate in the synthesis of Fluoxetine (HY-B0102) .
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Cat. No.: HY-79334R
CAS No.: 4254-15-3
(S)-(+)-1,2-Propanediol (Standard) is the analytical standard of (S)-(+)-1,2-Propanediol. This product is intended for research and analytical applications. (S)-(+)-1,2-Propanediol is an endogenous metabolite. (S)-(+)-1,2-Propanediol can be used as an organic solvent and diluent in drug preparations. (S)-(+)-1,2-Propanediol can also be used as a chiral synthetic intermediate and a substrate for enzyme research.
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Cat. No.: HY-169495
CAS No.: 53110-06-8
Target:  

Drug Intermediate

Research Areas:  

Others

ent-Corey PG-lactone diol is a versatile, chiral intermediate used in the preparation of PGs and PG analogs.
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Cat. No.: HY-W756265
(R)-(-)-N-Boc-3-pyrrolidinol-d4 is the d4-labeled (R)-(-)-N-Boc-3-pyrrolidinol (HY-W001294). (R)-(-)-N-Boc-3-pyrrolidinol is a chiral pyrrolidine derivative. After undergoing configuration inversion via the Mitsunobu reaction, (R)-(-)-N-Boc-3-pyrrolidinol can serve as a precursor for the (3S)-aryloxypyrrolidine fragment, which is used to construct key intermediates of FXa inhibitors (such as DX-9065a (HY-10722)) and various chiral drugs. (R)-(-)-N-Boc-3-pyrrolidinol can be applied in studies related to arrhythmia .
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Cat. No.: HY-W012618R
CAS No.: 93-54-9
Research Areas:  

Others

1-Phenyl-1-propanol (Standard) is the analytical standard of 1-Phenyl-1-propanol (HY-W012618). This product is intended for research and analytical applications. 1-Phenyl-1-propanol is an isomer of phenylpropanol. 1-Phenyl-1-propanol can serve as a fragrance or flavor enhancer, and as a chiral intermediate in the synthesis of Fluoxetine (HY-B0102) .
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Cat. No.: HY-N8275
CAS No.: 18951-85-4
(R)-(+)-Citronellic acid is a chiral carboxylic acid and can be used as a drug intermediate .
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Cat. No.: HY-W479432
CAS No.: 84621-34-1
Target:  

Drug Intermediate

Research Areas:  

Others

(R)-Methyl 2-(3-oxocyclopentyl)acetate is a chiral organic compound that can be used as a drug intermediate .
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Cat. No.: HY-W721183
CAS No.: 3056-44-8
Target:  

Drug Intermediate

Research Areas:  

Others

D-gluco-Hexodialdose,a glucose, is a chiral intermediate with multiple industrial applications. D-gluco-Hexodialdose is a building block for the synthesis of Organoboron monosaccharides.
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