(R)-1-(2-Chlorophenyl)-2-methoxy-2-oxoethyl (R)-2-(2-chlorophenyl)-2-(6,7-dihydrothieno[3,2-c]pyridin-5(4H)-yl)acetate

98%

Reagent Code: #229125
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CAS Number 1421283-60-4

science Other reagents with same CAS 1421283-60-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 490.4 g/mol
Formula C₂₄H₂₁Cl₂NO₄S
badge Registry Numbers
MDL Number MFCD28358804
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used in the pharmaceutical industry as an intermediate in the synthesis of anticoagulant drugs. It plays a key role in the production of potent platelet aggregation inhibitors, helping to prevent blood clot formation in cardiovascular treatments. Due to its chiral structure, it contributes to the selectivity and efficacy of the final drug compound, improving metabolic stability and target specificity. It is particularly valuable in developing therapies for patients at risk of stroke or myocardial infarction.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿27,750.00
inventory 100mg
10-20 days ฿47,170.00
inventory 1g
10-20 days ฿216,350.00
inventory 250mg
10-20 days ฿80,150.00

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(R)-1-(2-Chlorophenyl)-2-methoxy-2-oxoethyl (R)-2-(2-chlorophenyl)-2-(6,7-dihydrothieno[3,2-c]pyridin-5(4H)-yl)acetate
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Used in the pharmaceutical industry as an intermediate in the synthesis of anticoagulant drugs. It plays a key role in the production of potent platelet aggregation inhibitors, helping to prevent blood clot formation in cardiovascular treatments. Due to its chiral structure, it contributes to the selectivity and efficacy of the final drug compound, improving metabolic stability and target specificity. It is particularly valuable in developing therapies for patients at risk of stroke or myocardial infarct

Used in the pharmaceutical industry as an intermediate in the synthesis of anticoagulant drugs. It plays a key role in the production of potent platelet aggregation inhibitors, helping to prevent blood clot formation in cardiovascular treatments. Due to its chiral structure, it contributes to the selectivity and efficacy of the final drug compound, improving metabolic stability and target specificity. It is particularly valuable in developing therapies for patients at risk of stroke or myocardial infarction.

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