1. Home
  2. 1,6-Naphthyridine, 2-chloro-5-methyl-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

1,6-Naphthyridine, 2-chloro-5-methyl-

Clc1ccc2c(n1)ccnc2C Request for Quotation
Chemical Name: 1,6-Naphthyridine, 2-chloro-5-methyl-
CAS Number: 140692-93-9
Product Number: AG001COY(AGN-PC-0KT5F5)
Synonyms:
MDL No:
Molecular Formula: C9H7ClN2
Molecular Weight: 178.6183

Identification/Properties

Computed Properties
Molecular Weight:
178.619g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
178.03g/mol
Monoisotopic Mass:
178.03g/mol
Topological Polar Surface Area:
25.8A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
163
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:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


2-Chloro-5-methyl-1,6-naphthyridine is a versatile compound widely used in chemical synthesis. Its unique structure and reactivity make it a valuable building block for the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. In organic synthesis, this compound serves as a key intermediate in the preparation of heterocyclic compounds through cyclization reactions. Its halogen substituent provides opportunities for further functionalization, allowing for the synthesis of diverse molecular structures. Additionally, 2-Chloro-5-methyl-1,6-naphthyridine can be employed in cross-coupling reactions to form carbon-carbon or carbon-heteroatom bonds, enabling the synthesis of complex organic molecules with high efficiency. Its strategic position in multi-step synthesis routes makes it a valuable tool for medicinal and materials chemists seeking to design and develop novel compounds with specific properties and functions.