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1-Naphthylamine - Analytical Reagent,99.0%, high purity , CAS No.134-32-7
Basic Description
Synonyms
BRN 0386133 | 1-naphthyl amine | alpha-Naftalamin | RCRA waste no. U167 | 1-amino napthalene | 1-Naftilamina | 1-Naphthylamin [German] | CI Azoic Diazo Component 114 | STK301604 | 1-Aminonaftalen [Czech] | 1-Naftylamin [Czech] | 1-Naphthylamine, analytica
Specifications & Purity
AR, ≥99%
Storage Temp
Store at 2-8°C,Argon charged
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Grade
AR
Product Description
1-Naphthylamine has been used in the synthesis of Pitnot-2, an inactive analog of clathrin inhibitor Pitstop 2.
It can also be used as a starting material to synthesize:
· [(S)-HY-Phos], a novel chiral phosphine-phosphoramidite ligand for use in rhodium-catalyzed asymmetric hydrogenation of various functionalized olefins.
· N-(naphthalen-1-yl)picolinamide.
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Benzenoids
Class
Naphthalenes
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Naphthalenes
Alternative Parents
Primary amines Organopnictogen compounds Hydrocarbon derivatives
Molecular Framework
Aromatic homopolycyclic compounds
Substituents
Naphthalene - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Organonitrogen compound - Amine - Aromatic homopolycyclic compound
Description
This compound belongs to the class of organic compounds known as naphthalenes. These are compounds containing a naphthalene moiety, which consists of two fused benzene rings.
External Descriptors
naphthylamine
Data sources
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
Associated Targets(Human)
Associated Targets(non-human)
Mechanisms of Action
Mechanism of Action
Action Type
target ID
Target Name
Target Type
Target Organism
Binding Site Name
References
Names and Identifiers
Pubchem Sid
504751709
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/504751709
IUPAC Name
naphthalen-1-amine
INCHI
InChI=1S/C10H9N/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-7H,11H2
InChIKey
RUFPHBVGCFYCNW-UHFFFAOYSA-N
Smiles
C1=CC=C2C(=C1)C=CC=C2N
Isomeric SMILES
C1=CC=C2C(=C1)C=CC=C2N
WGK Germany
2
RTECS
QM1400000
UN Number
2077
Packing Group
III
Molecular Weight
143.19
Beilstein
386133
Reaxy-Rn
386133
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=386133&ln=
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
Solubility
Solubility in dilute Acetic acid almost transparency;
Sensitivity
Light and Air sensitive
Flash Point(°F)
314.6 °F
Flash Point(°C)
157℃
Boil Point(°C)
301°C
Melt Point(°C)
50°C
Molecular Weight
143.180 g/mol
XLogP3
2.200
Hydrogen Bond Donor Count
1
Hydrogen Bond Acceptor Count
1
Rotatable Bond Count
0
Exact Mass
143.073 Da
Monoisotopic Mass
143.073 Da
Topological Polar Surface Area
26.000 Ų
Heavy Atom Count
11
Formal Charge
0
Complexity
133.000
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
The total count of all stereochemical bonds
0
Covalently-Bonded Unit Count
1
Citations of This Product
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