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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)-

3H-Benz[e]indole-2-carbonitrile, 8-(dipropylamino)-6,7,8,9-tetrahydro-,monohydrochloride, (8R)-

CCCN([C@@H]1CCc2c(C1)c1cc([nH]c1cc2)C#N)CCC.Cl Request for Quotation
Chemical Name: 3H-Benz[e]indole-2-carbonitrile, 8-(dipropylamino)-6,7,8,9-tetrahydro-,monohydrochloride, (8R)-
CAS Number: 149654-41-1
Product Number: AG00ATFF(AGN-PC-0Q3LPG)
Synonyms:
MDL No: MFCD00920890
Molecular Formula: C19H26ClN3
Molecular Weight: 331.8828

Identification/Properties

Computed Properties
Molecular Weight:
331.888g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
5
Exact Mass:
331.182g/mol
Monoisotopic Mass:
331.182g/mol
Topological Polar Surface Area:
42.8A^2
Heavy Atom Count:
23
Formal Charge:
0
Complexity:
406
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


3H-Benz[e]indole-2-carbonitrile, 8-(dipropylamino)-6,7,8,9-tetrahydro-, hydrochloride (1:1), (8R)- is a valuable compound utilized in chemical synthesis for its unique properties and versatile applications. This compound serves as a key building block in the creation of pharmaceutical intermediates and fine chemicals. Its chiral nature, specifically the (8R) configuration, makes it particularly advantageous in asymmetric synthesis processes, enabling the production of enantiomerically pure compounds. By incorporating this compound into various reactions, chemists can access a wide range of structurally diverse molecules with high levels of stereocontrol. Furthermore, the hydrochloride salt form enhances the compound's solubility and stability, facilitating its use in aqueous reactions and pharmaceutical formulations. In summary, 3H-Benz[e]indole-2-carbonitrile, 8-(dipropylamino)-6,7,8,9-tetrahydro-, hydrochloride (1:1), (8R)- is a crucial component in modern chemical synthesis, offering synthetic chemists the opportunity to efficiently access complex molecules with precise stereochemistry.