3-Chloro-5-methoxyaniline

CAS: 10272-06-7 | OR313073 | 3-Chloro-5-methoxyaniline

Catalogue Number OR313073

Synonym(s):

3-Chloro-5-methoxyaniline (CAS: 10272-06-7) is an organic building block used in the synthesis of pharmaceutical and agrochemical components. It can be used as an electrophilic partner in... Read More

CAS Number

10272-06-7

Commodity Code

2921410090

MDL Number

MFCD11035922

Formula Weight
157.60 g/mol
Chemical Hazard
Harmful/Irritant
GHS
Hazard Statements
May cause respiratory irritation.|Harmful if swallowed.|Causes skin irritation.|Causes serious eye irritation.
Precautionary Statements
Use only outdoors or in a well-ventilated area.|Avoid breathing dust/fumes.|Wash all exposed external body areas thoroughly after handling.|Do not eat: hazard.Use only outdoors or in a well-ventilated area.|Avoid breathing dust/fumes.|Wash all exposed external body areas thoroughly after handling.|Do not eat
drink or smoke when using this product.|Wear protective gloves: hazard. drink or smoke when using this product.|Wear protective gloves
protective clothing: hazard. protective clothing
eye protection and: hazard. eye protection and
MSDS
View MSDS
Typical Batch COA
View
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Size
UK Stock
UK stock will be shipped internationally
US Stock
US stock is for US shipping only
Price
Quantity
Add to Basket
1g
5 Packs in stock.
In Stock
£37.00
5g
1 Packs in stock.
3 Packs in stock.
£109.00
25g
Out of Stock
Out of Stock
£517.00
Size 1g
Price £37.00
UK Stock 5 Packs in stock.
US Stock In Stock
Size 5g
Price £109.00
UK Stock 1 Packs in stock.
US Stock 3 Packs in stock.
Size 25g
Price £517.00
UK Stock Out of Stock
US Stock Out of Stock

Product Description

3-Chloro-5-methoxyaniline (CAS: 10272-06-7) is an organic building block used in the synthesis of pharmaceutical and agrochemical components. It can be used as an electrophilic partner in a variety of palladium-catalysed cross-coupling reactions and as a nucleophilic reagent in amide couplings. It has been used in the synthesis of ALK2 kinase inhibitors for the treatment of cancer,[1] and in the synthesis of small molecule KRAS G12C inhibitors.[2]

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1) https://worldwide.espacenet.com/patent/search/family/064659499/publication/US11661426B2?q=pn%3DUS11661426

2) https://worldwide.espacenet.com/patent/search/family/083847491/publication/WO2022232320A1?q=pn%3DWO2022232320