(9H-Fluoren-9-yl)methyl (S)-(1-(5,6,7,8-tetrahydronaphthalen-1-yl)propan-2-yl)carbamate

95%

Reagent Code: #196992
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CAS Number 2349890-61-3

science Other reagents with same CAS 2349890-61-3

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inventory_2 Storage & Handling
Storage 2-8°C, drying away from light

description Product Description

Used in pharmaceutical synthesis as an intermediate for producing selective estrogen receptor modulators (SERMs). It plays a key role in the development of drugs targeting hormone-dependent conditions such as breast cancer and osteoporosis. The compound's structure, featuring an Fmoc-protected chiral amine derived from tetrahydronaphthalene, allows for chiral specificity and enhanced binding affinity in final active pharmaceutical ingredients. Commonly employed in research settings for optimizing drug candidates with improved metabolic stability and tissue selectivity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿33,960.00
inventory 250mg
10-20 days ฿45,980.00

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(9H-Fluoren-9-yl)methyl (S)-(1-(5,6,7,8-tetrahydronaphthalen-1-yl)propan-2-yl)carbamate
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Used in pharmaceutical synthesis as an intermediate for producing selective estrogen receptor modulators (SERMs). It plays a key role in the development of drugs targeting hormone-dependent conditions such as breast cancer and osteoporosis. The compound's structure, featuring an Fmoc-protected chiral amine derived from tetrahydronaphthalene, allows for chiral specificity and enhanced binding affinity in final active pharmaceutical ingredients. Commonly employed in research settings for optimizing drug ca

Used in pharmaceutical synthesis as an intermediate for producing selective estrogen receptor modulators (SERMs). It plays a key role in the development of drugs targeting hormone-dependent conditions such as breast cancer and osteoporosis. The compound's structure, featuring an Fmoc-protected chiral amine derived from tetrahydronaphthalene, allows for chiral specificity and enhanced binding affinity in final active pharmaceutical ingredients. Commonly employed in research settings for optimizing drug candidates with improved metabolic stability and tissue selectivity.

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