tert-Butyl 3-amino-6,6-dimethyl-2-(propionyloxy)-4,6-dihydropyrrolo[3,4-c]pyrazole-5(2H)-carboxylate

97%

Reagent Code: #151444
fingerprint
CAS Number 2007916-02-9

science Other reagents with same CAS 2007916-02-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 324.38 g/mol
Formula C₁₅H₂₄N₄O₄
badge Registry Numbers
MDL Number MFCD30471861
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structure allows for selective modification, making it valuable in creating biologically active molecules. Commonly employed in research settings for designing drugs that require a sterically hindered amine group and a protected heterocyclic core. Also utilized in the preparation of protease inhibitors and antiviral agents due to its ability to mimic peptide motifs while enhancing metabolic stability.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,050.00
inventory 250mg
10-20 days ฿11,710.00
inventory 1g
10-20 days ฿37,760.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
tert-Butyl 3-amino-6,6-dimethyl-2-(propionyloxy)-4,6-dihydropyrrolo[3,4-c]pyrazole-5(2H)-carboxylate
No image available

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structure allows for selective modification, making it valuable in creating biologically active molecules. Commonly employed in research settings for designing drugs that require a sterically hindered amine group and a protected heterocyclic core. Also utilized in the preparation of protease inhibitors and antiviral agents due to its ability to mimi

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structure allows for selective modification, making it valuable in creating biologically active molecules. Commonly employed in research settings for designing drugs that require a sterically hindered amine group and a protected heterocyclic core. Also utilized in the preparation of protease inhibitors and antiviral agents due to its ability to mimic peptide motifs while enhancing metabolic stability.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...