4-Methoxyphenylhydrazine hydrochloride

98%

Reagent Code: #80349
label
Alias 4-methoxyphenylhydrazine hydrochloride; p-methoxyphenylhydrazine hydrochloride
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CAS Number 19501-58-7

science Other reagents with same CAS 19501-58-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 174.63 g/mol
Formula C₇H₁₀N₂OHCl
badge Registry Numbers
EC Number 243-115-3
MDL Number MFCD00012945
thermostat Physical Properties
Melting Point 160-162 °C (dec.)(lit.)
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

Used primarily in organic synthesis, this compound serves as a key reagent in the preparation of various heterocyclic compounds, particularly indoles. It is employed in the Fischer indole synthesis, a widely used method for creating indole derivatives, which are important in pharmaceutical and agrochemical industries. Additionally, it finds application in the synthesis of dyes and pigments due to its ability to form stable intermediates. Its role in the development of biologically active molecules makes it valuable in medicinal chemistry research.

format_list_bulleted Product Specification

Test Parameter Specification
Melting point 155-163
Purity (HPLC) 98-100%
Purity (Titration with AgNO3) 97.5-102.5%
Appearance White to purple powder
Infrared Spectrometry Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,390.00
inventory 25g
10-20 days ฿5,200.00
inventory 100g
10-20 days ฿12,460.00
inventory 500g
10-20 days ฿56,360.00

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4-Methoxyphenylhydrazine hydrochloride
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Used primarily in organic synthesis, this compound serves as a key reagent in the preparation of various heterocyclic compounds, particularly indoles. It is employed in the Fischer indole synthesis, a widely used method for creating indole derivatives, which are important in pharmaceutical and agrochemical industries. Additionally, it finds application in the synthesis of dyes and pigments due to its ability to form stable intermediates. Its role in the development of biologically active molecules makes

Used primarily in organic synthesis, this compound serves as a key reagent in the preparation of various heterocyclic compounds, particularly indoles. It is employed in the Fischer indole synthesis, a widely used method for creating indole derivatives, which are important in pharmaceutical and agrochemical industries. Additionally, it finds application in the synthesis of dyes and pigments due to its ability to form stable intermediates. Its role in the development of biologically active molecules makes it valuable in medicinal chemistry research.

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