1-Chloromethyl-1H-1,2,4-triazole hydrochloride

97%

Reagent Code: #163878
label
Alias Chloromethyltriazole hydrochloride; Related CAS No.: 114369-18-5
fingerprint
CAS Number 84387-61-1

science Other reagents with same CAS 84387-61-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 154 g/mol
Formula C₃H₄ClN₃•HCl
badge Registry Numbers
MDL Number MFCD00964947
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of triazole-based pharmaceuticals, particularly antifungal and antiviral agents. Its reactivity allows for the introduction of the 1,2,4-triazole ring into larger molecules, which is a common structural motif in drugs targeting fungal cytochrome P450 enzymes. Also employed in agrochemicals for the development of fungicides and plant growth regulators. The chloromethyl group facilitates alkylation reactions, making it valuable in heterocyclic chemistry for building complex bioactive molecules.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance white to light yellow solid
Purity (%) 96.5-100%
Infrared spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,980.00
inventory 5g
10-20 days ฿25,600.00
inventory 1g
10-20 days ฿9,800.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
1-Chloromethyl-1H-1,2,4-triazole hydrochloride
No image available
Used as a key intermediate in the synthesis of triazole-based pharmaceuticals, particularly antifungal and antiviral agents. Its reactivity allows for the introduction of the 1,2,4-triazole ring into larger molecules, which is a common structural motif in drugs targeting fungal cytochrome P450 enzymes. Also employed in agrochemicals for the development of fungicides and plant growth regulators. The chloromethyl group facilitates alkylation reactions, making it valuable in heterocyclic chemistry for building
Used as a key intermediate in the synthesis of triazole-based pharmaceuticals, particularly antifungal and antiviral agents. Its reactivity allows for the introduction of the 1,2,4-triazole ring into larger molecules, which is a common structural motif in drugs targeting fungal cytochrome P450 enzymes. Also employed in agrochemicals for the development of fungicides and plant growth regulators. The chloromethyl group facilitates alkylation reactions, making it valuable in heterocyclic chemistry for building complex bioactive molecules.
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...