Methyl2-amino-5-iodothiazole-4-carboxylate

97%

Reagent Code: #213951
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CAS Number 1235034-76-0

science Other reagents with same CAS 1235034-76-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 284.08 g/mol
Formula C₅H₅IN₂O₂S
badge Registry Numbers
MDL Number MFCD28099756
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and anticancer agents. Its structure supports the formation of biologically active molecules by serving as a building block in heterocyclic chemistry. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the presence of reactive amino and ester groups, allowing easy modification. Also utilized in the preparation of kinase inhibitors and other targeted therapies. The iodine atom enables further functionalization through cross-coupling reactions, making it valuable in drug discovery and development.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,290.00
inventory 250mg
10-20 days ฿5,740.00
inventory 1g
10-20 days ฿21,100.00
Methyl2-amino-5-iodothiazole-4-carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and anticancer agents. Its structure supports the formation of biologically active molecules by serving as a building block in heterocyclic chemistry. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the presence of reactive amino and ester groups, allowing easy modification. Also utilized in the preparation of kinase inhibitors and other targeted t

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and anticancer agents. Its structure supports the formation of biologically active molecules by serving as a building block in heterocyclic chemistry. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the presence of reactive amino and ester groups, allowing easy modification. Also utilized in the preparation of kinase inhibitors and other targeted therapies. The iodine atom enables further functionalization through cross-coupling reactions, making it valuable in drug discovery and development.

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