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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)-

5-chloro-1,2,3,4-tetrahydro-1,6-naphthyridine

Clc1nccc2c1CCCN2 Request for Quotation
Chemical Name: 5-chloro-1,2,3,4-tetrahydro-1,6-naphthyridine
CAS Number: 98490-61-0
Product Number: AG00IK40(AGN-PC-07HAYR)
Synonyms:
MDL No:
Molecular Formula: C8H9ClN2
Molecular Weight: 168.6235

Identification/Properties

Computed Properties
Molecular Weight:
168.624g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
168.045g/mol
Monoisotopic Mass:
168.045g/mol
Topological Polar Surface Area:
24.9A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
140
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Chloro-1,2,3,4-tetrahydro-1,6-naphthyridine, commonly referred to as $name$, is a versatile compound with significant utility in chemical synthesis. One notable application of this compound is as a key building block in the production of pharmaceutical intermediates. By incorporating $name$ into synthetic pathways, chemists can access a variety of structurally diverse molecules that hold promise for drug discovery and development. The unique reactivity and structural characteristics of 5-Chloro-1,2,3,4-tetrahydro-1,6-naphthyridine make it a valuable tool for accessing complex molecular architectures efficiently and selectively. Additionally, its presence in the synthesized molecules can impart desirable properties or functions, further enhancing their potential utility in various applications.