6-Chloro-4-methoxynicotinaldehyde

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Reagent Code: #120544
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CAS Number 1256823-05-8

science Other reagents with same CAS 1256823-05-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 171.58 g/mol
Formula C₇H₆ClNO₂
badge Registry Numbers
MDL Number MFCD18255526
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

Used as an intermediate in the synthesis of various pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs). It plays a role in the production of compounds with potential therapeutic applications, such as anti-inflammatory, antiviral, or anticancer agents. Additionally, it is utilized in organic chemistry research for constructing complex molecules due to its reactive aldehyde and chloro groups, which facilitate further chemical modifications. Its methoxy group also contributes to its utility in creating structurally diverse compounds for drug discovery and development.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,095.00
inventory 250mg
10-20 days ฿6,840.00
inventory 1g
10-20 days ฿14,022.00

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6-Chloro-4-methoxynicotinaldehyde
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Used as an intermediate in the synthesis of various pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs). It plays a role in the production of compounds with potential therapeutic applications, such as anti-inflammatory, antiviral, or anticancer agents. Additionally, it is utilized in organic chemistry research for constructing complex molecules due to its reactive aldehyde and chloro groups, which facilitate further chemical modifications. Its methoxy group also c

Used as an intermediate in the synthesis of various pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs). It plays a role in the production of compounds with potential therapeutic applications, such as anti-inflammatory, antiviral, or anticancer agents. Additionally, it is utilized in organic chemistry research for constructing complex molecules due to its reactive aldehyde and chloro groups, which facilitate further chemical modifications. Its methoxy group also contributes to its utility in creating structurally diverse compounds for drug discovery and development.

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