118-46-7 | 8-Amino-2-naphthol

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$10.00	$7.00
5g	98%	in stock	$20.00	$14.00
25g	98%	in stock	$58.00	$40.00

Description

• Catalog Number: AD34622
• Chemical Name: 8-Amino-2-naphthol
• CAS Number: 118-46-7
• Molecular Formula: C10H9NO
• Molecular Weight: 159.1846
• MDL Number: MFCD00004031
• SMILES: Oc1ccc2c(c1)c(N)ccc2

Computed Properties

• Complexity: 160
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 12
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 2
• XLogP3: 1.6

Upstream Synthesis Route

8-Amino-2-naphthalenol, also known as 8-amino-2-naphthol or 2-amino-1-naphthol, is a versatile compound widely used in chemical synthesis due to its unique properties. This aromatic amine derivative plays a crucial role in various industrial processes and research applications.The primary application of 8-Amino-2-naphthalenol lies in its utility as a key intermediate in the synthesis of dyes and pigments. Its ability to undergo selective functionalization reactions makes it an essential building block for the production of vibrant and long-lasting colorants used in textiles, plastics, and other materials.Furthermore, 8-Amino-2-naphthalenol serves as a valuable precursor in pharmaceutical chemistry. Its structural flexibility allows for the introduction of specific functional groups, enabling the synthesis of novel drug candidates and therapeutic agents. Additionally, this compound is employed in the preparation of fluorescent probes and molecular markers for biological imaging and analysis.In the field of material science, 8-Amino-2-naphthalenol is utilized in the synthesis of advanced polymers and specialty chemicals with tailored properties. Its aromatic nature and reactivity contribute to the development of high-performance materials for various industrial applications, including coatings, adhesives, and electronics.Overall, the significance of 8-Amino-2-naphthalenol in chemical synthesis lies in its versatility, enabling the creation of diverse compounds with enhanced functionalities and applications across multiple industries.

Literature

• 5-Amino-1-naphthol: two-dimensional sheets built up from R(4)(4)(18) rings formed by O-H...N, N-H...O and pi-pi interactions.

  Acta crystallographica. Section C, Crystal structure communications 20091101

• Non-biaryl atropisomers in organocatalysis.

  Chemistry (Weinheim an der Bergstrasse, Germany) 20060807