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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)-

(S)-4-Fluoro-indan-1-ylamine HCl

N[C@H]1CCc2c1cccc2F Request for Quotation
Chemical Name: (S)-4-Fluoro-indan-1-ylamine HCl
CAS Number: 946053-90-3
Product Number: AG00IIDZ(AGN-PC-0WA2ZG)
Synonyms:
MDL No:
Molecular Formula: C9H10FN
Molecular Weight: 151.1808

Identification/Properties

Computed Properties
Molecular Weight:
151.184g/mol
XLogP3:
1.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
151.08g/mol
Monoisotopic Mass:
151.08g/mol
Topological Polar Surface Area:
26A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
149
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:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


(S)-4-Fluoro-2,3-dihydro-1H-inden-1-amine is a versatile compound frequently utilized in chemical synthesis as a chiral building block. Due to its unique structure and stereochemistry, this compound plays a crucial role as a key intermediate in the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals. Its chiral nature enables it to impart specific stereochemical properties to the final products, making it a valuable tool for the production of enantiomerically pure compounds with desired biological activity. In addition, (S)-4-Fluoro-2,3-dihydro-1H-inden-1-amine can be involved in the creation of complex organic molecules through asymmetric synthesis, contributing to the development of new materials and drug candidates. Its application in chemical synthesis showcases its importance in modern organic chemistry research and industrial manufacturing processes.