3,5-Dichloro-2-methoxybenzoic acid

98%

Reagent Code: #171212
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CAS Number 22775-37-7

science Other reagents with same CAS 22775-37-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 221.04 g/mol
Formula C₈H₆Cl₂O₃
badge Registry Numbers
MDL Number MFCD00017545
thermostat Physical Properties
Boiling Point 333.2°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It plays a key role in the production of selective herbicides, particularly those targeting broadleaf weeds. Its structure allows for effective derivatization in the development of plant growth regulators. Additionally, it is employed in research settings for the preparation of bioactive molecules and functionalized aromatic compounds. Its chloro and methoxy groups enhance reactivity in coupling reactions, making it valuable in organic synthesis.

Available Sizes & Pricing

Size Availability Unit Price Quantity
25mg
10-20 days ฿180.00
100mg
10-20 days ฿410.00
250mg
10-20 days ฿990.00
1g
10-20 days ฿2,410.00
5g
10-20 days ฿9,620.00
25g
10-20 days ฿45,990.00
3,5-Dichloro-2-methoxybenzoic acid
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Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It plays a key role in the production of selective herbicides, particularly those targeting broadleaf weeds. Its structure allows for effective derivatization in the development of plant growth regulators. Additionally, it is employed in research settings for the preparation of bioactive molecules and functionalized aromatic compounds. Its chloro and methoxy groups enhance reactivity in coupling reactions, making it

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It plays a key role in the production of selective herbicides, particularly those targeting broadleaf weeds. Its structure allows for effective derivatization in the development of plant growth regulators. Additionally, it is employed in research settings for the preparation of bioactive molecules and functionalized aromatic compounds. Its chloro and methoxy groups enhance reactivity in coupling reactions, making it valuable in organic synthesis.

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