(S)-1-(4H-[1,2,4]-triazol-3-yl)ethylamine hydrochloride

Reagent Code: #37927
fingerprint
CAS Number 1225462-32-7

science Other reagents with same CAS 1225462-32-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 148.59 g/mol
Formula C₄H₉ClN₄
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used in pharmaceutical research, this compound serves as a key intermediate in the synthesis of various biologically active molecules. It is particularly valuable in developing antifungal and antimicrobial agents due to its triazole moiety, which is known for its efficacy in inhibiting fungal enzymes. Additionally, it finds application in the preparation of chiral compounds, leveraging its stereochemistry to produce enantiomerically pure drugs. Its role in medicinal chemistry is crucial for designing compounds with improved therapeutic properties and reduced side effects.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿9,000.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(S)-1-(4H-[1,2,4]-triazol-3-yl)ethylamine hydrochloride
No image available

Used in pharmaceutical research, this compound serves as a key intermediate in the synthesis of various biologically active molecules. It is particularly valuable in developing antifungal and antimicrobial agents due to its triazole moiety, which is known for its efficacy in inhibiting fungal enzymes. Additionally, it finds application in the preparation of chiral compounds, leveraging its stereochemistry to produce enantiomerically pure drugs. Its role in medicinal chemistry is crucial for designing com

Used in pharmaceutical research, this compound serves as a key intermediate in the synthesis of various biologically active molecules. It is particularly valuable in developing antifungal and antimicrobial agents due to its triazole moiety, which is known for its efficacy in inhibiting fungal enzymes. Additionally, it finds application in the preparation of chiral compounds, leveraging its stereochemistry to produce enantiomerically pure drugs. Its role in medicinal chemistry is crucial for designing compounds with improved therapeutic properties and reduced side effects.

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...