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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-Amino-6-fluorochroman Hydrochloride

Fc1ccc2c(c1)[C@@H](N)CCO2.Cl Request for Quotation
Chemical Name: (S)-4-Amino-6-fluorochroman Hydrochloride
CAS Number: 1260609-97-9
Product Number: AG000QWD(AGN-PC-0WA2Z6)
Synonyms:
MDL No: MFCD15474861
Molecular Formula: C9H11ClFNO
Molecular Weight: 203.6411

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
203.641g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
203.051g/mol
Monoisotopic Mass:
203.051g/mol
Topological Polar Surface Area:
35.2A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
165
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

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


The compound 2H-1-Benzopyran-4-amine, 6-fluoro-3,4-dihydro-, hydrochloride (1:1), (4S)- is utilized in chemical synthesis as a key reagent for the preparation of various pharmacologically active molecules. This compound is specifically valued for its ability to serve as a building block in the synthesis of potential drug candidates targeting specific biological pathways. Its stereochemistry, in the form of the (4S)- enantiomer, plays a crucial role in determining the activity and selectivity of the final synthesized compounds. In the realm of chemical research and drug discovery, the strategic incorporation of this compound facilitates the creation of diverse chemical libraries for screening purposes, ultimately paving the way for the development of novel therapeutic agents with enhanced efficacy and reduced side effects.