5-(Aminomethyl)thiazole dihydrochloride

97%

Reagent Code: #137298
fingerprint
CAS Number 1215372-00-1

science Other reagents with same CAS 1215372-00-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 187.09 g/mol
Formula C₄H₆N₂S
badge Registry Numbers
MDL Number MFCD16090013
thermostat Physical Properties
Melting Point 215-222 °C
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of thiazole-based drugs with antimicrobial and antiviral properties. Commonly employed in the preparation of active pharmaceutical ingredients (APIs) where the aminomethyl group facilitates coupling reactions in peptide-like structures. Also utilized in the design of kinase inhibitors and other biologically active molecules due to its ability to enhance binding affinity with target enzymes. Its hydrochloride salt form improves solubility and stability in aqueous reaction environments, making it suitable for use in polar solvents during drug synthesis.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿5,300.00
inventory 1g
10-20 days ฿9,070.00
inventory 5g
10-20 days ฿27,140.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
5-(Aminomethyl)thiazole dihydrochloride
No image available
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of thiazole-based drugs with antimicrobial and antiviral properties. Commonly employed in the preparation of active pharmaceutical ingredients (APIs) where the aminomethyl group facilitates coupling reactions in peptide-like structures. Also utilized in the design of kinase inhibitors and other biologically active molecules due to its ability to enhance binding affinity with target enzymes. Its hydrochloride salt
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of thiazole-based drugs with antimicrobial and antiviral properties. Commonly employed in the preparation of active pharmaceutical ingredients (APIs) where the aminomethyl group facilitates coupling reactions in peptide-like structures. Also utilized in the design of kinase inhibitors and other biologically active molecules due to its ability to enhance binding affinity with target enzymes. Its hydrochloride salt form improves solubility and stability in aqueous reaction environments, making it suitable for use in polar solvents during drug synthesis.
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...