118-04-7 | 2-(3-Amino-4-chlorobenzoyl)benzoic acid

Packsize	Purity	Availability	Price	Discounted Price
5g	97%	in stock	$23.00	$16.00
10g	97%	in stock	$29.00	$20.00
25g	97%	in stock	$55.00	$38.00
100g	97%	in stock	$153.00	$107.00
500g	97%	in stock	$417.00	$292.00

Description

• Catalog Number: AB51380
• Chemical Name: 2-(3-Amino-4-chlorobenzoyl)benzoic acid
• CAS Number: 118-04-7
• Molecular Formula: C14H10ClNO3
• Molecular Weight: 275.6871
• MDL Number: MFCD00007672
• SMILES: O=C(c1ccccc1C(=O)O)c1ccc(c(c1)N)Cl
• NSC Number: 74496

Computed Properties

• Complexity: 361
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 19
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 3
• XLogP3: 2.7

Upstream Synthesis Route

2-(3-Amino-4-chlorobenzoyl)benzoic acid, also known as $name$, plays a crucial role in chemical synthesis as a versatile building block. This compound is commonly utilized in organic chemistry for the production of various pharmaceuticals, agrochemicals, and functional materials. $name$ serves as a key intermediate in the synthesis of important organic molecules due to its unique structural properties. Its presence enables the introduction of specific functional groups, such as amino and chloro substituents, into the target compounds. This allows chemists to control and modify the reactivity, solubility, and biological activity of the final products.In chemical synthesis, $name$ can be selectively modified by reacting with different reagents to form new compounds with diverse properties. The amino group can undergo various transformations, such as acylation, alkylation, or reduction, leading to the creation of structurally complex molecules. Additionally, the chloro group provides an opportunity for further derivatization through substitution reactions, expanding the structural diversity of the synthesized compounds.Overall, the strategic incorporation of 2-(3-Amino-4-chlorobenzoyl)benzoic acid in chemical synthesis enables the efficient construction of intricate molecular scaffolds with tailored functionalities, making it an indispensable component in the synthesis of advanced materials and bioactive compounds.