2-Amino-3-methoxybenzaldehyde

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Reagent Code: #42610
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CAS Number 70127-96-7

science Other reagents with same CAS 70127-96-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 151.1600 g/mol
Formula C₈H₉NO₂
badge Registry Numbers
MDL Number MFCD09999245
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals, including potential anticancer agents and anti-inflammatory drugs. It is also utilized in the synthesis of dyes and pigments due to its aldehyde and amino functional groups, which allow for versatile chemical modifications. Additionally, it plays a role in the development of organic electronic materials, contributing to the advancement of optoelectronic devices. Its methoxy group further enhances its reactivity, making it valuable in complex chemical transformations.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,618.00

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2-Amino-3-methoxybenzaldehyde
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Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals, including potential anticancer agents and anti-inflammatory drugs. It is also utilized in the synthesis of dyes and pigments due to its aldehyde and amino functional groups, which allow for versatile chemical modifications. Additionally, it plays a role in the development of organic electronic materials, contributing to the advancement of optoelectronic devices. Its methoxy group

Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals, including potential anticancer agents and anti-inflammatory drugs. It is also utilized in the synthesis of dyes and pigments due to its aldehyde and amino functional groups, which allow for versatile chemical modifications. Additionally, it plays a role in the development of organic electronic materials, contributing to the advancement of optoelectronic devices. Its methoxy group further enhances its reactivity, making it valuable in complex chemical transformations.

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