naphthalene-1,2-diamine


Chemical Name: naphthalene-1,2-diamine
CAS Number: 938-25-0
Product Number: AG00GRJQ(AGN-PC-0WAJ6A)
Synonyms:
MDL No:
Molecular Formula: C10H10N2
Molecular Weight: 158.1998

Identification/Properties


Computed Properties
Molecular Weight:
158.204g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
158.084g/mol
Monoisotopic Mass:
158.084g/mol
Topological Polar Surface Area:
52A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
158
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information


GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319
Precautionary Statements:
P264-P280-P302+P352-P305+P351+P338-P332+P313-P337+P313-P362
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



1,2-Naphthalenediamine, also known as 1,2-diaminonaphthalene, plays a crucial role in chemical synthesis as a versatile building block in the production of various organic compounds. This compound is commonly used in the synthesis of dyes, pharmaceuticals, and agrochemicals due to its reactivity and ability to undergo a variety of chemical transformations.In chemical synthesis, 1,2-naphthalenediamine serves as a key intermediate in the preparation of numerous azo dyes. By reacting with diazonium salts derived from aromatic amines, this compound can form vibrant colored dyes that are widely used in the textile, printing, and food industries. Additionally, the ability of 1,2-naphthalenediamine to undergo diazotization reactions makes it a valuable precursor in the synthesis of various pharmaceutical compounds, such as antimalarial and anticancer drugs.Furthermore, 1,2-naphthalenediamine is utilized in the development of agrochemicals, specifically in the creation of pesticides and herbicides. Through selective chemical modifications, this compound can be transformed into active ingredients that exhibit pesticidal properties, contributing to the protection of crops and enhancement of agricultural productivity.Overall, the application of 1,2-naphthalenediamine in chemical synthesis showcases its significance as a fundamental building block in the creation of diverse organic molecules with valuable industrial applications.