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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)-

3-Quinolinecarbonitrile, 2-chloro-5,6,7,8-tetrahydro-

N#Cc1cc2CCCCc2nc1Cl Request for Quotation
Chemical Name: 3-Quinolinecarbonitrile, 2-chloro-5,6,7,8-tetrahydro-
CAS Number: 65242-27-5
Product Number: AG00EDXR(AGN-PC-0KZYCG)
Synonyms:
MDL No:
Molecular Formula: C10H9ClN2
Molecular Weight: 192.6449

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
192.646g/mol
XLogP3:
2.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
192.045g/mol
Monoisotopic Mass:
192.045g/mol
Topological Polar Surface Area:
36.7A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
232
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


2-Chloro-5,6,7,8-tetrahydroquinoline-3-carbonitrile is a versatile compound widely used in chemical synthesis. Its unique structure and reactivity make it a valuable building block in organic chemistry. This compound serves as an important intermediate in the synthesis of various biologically active molecules, pharmaceuticals, and agrochemicals. Specifically, it can be employed in the development of new drugs, pesticides, and materials due to its ability to participate in diverse chemical reactions such as nucleophilic substitution, condensation, and cyclization. Additionally, its presence of both a cyano group and a chloro group provides opportunities for further functionalization, allowing for the creation of complex molecular structures. In summary, 2-Chloro-5,6,7,8-tetrahydroquinoline-3-carbonitrile plays a crucial role in the production of valuable compounds with a wide range of applications in various industries.