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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)-6-Chlorochroman-4-amine hydrochloride

Clc1ccc2c(c1)[C@@H](N)CCO2.Cl Request for Quotation
Chemical Name: (S)-6-Chlorochroman-4-amine hydrochloride
CAS Number: 1956436-48-8
Product Number: AG00I3JR(AGN-PC-0WAMIQ)
Synonyms:
MDL No:
Molecular Formula: C9H11Cl2NO
Molecular Weight: 220.0957

Identification/Properties

Computed Properties
Molecular Weight:
220.093g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
219.022g/mol
Monoisotopic Mass:
219.022g/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


(S)-6-Chlorochroman-4-amine hydrochloride is a versatile compound widely utilized in chemical synthesis. Its primary application lies in its role as a chiral building block in the preparation of various pharmaceuticals, agrochemicals, and other fine chemicals. Due to its unique stereochemistry, (S)-6-Chlorochroman-4-amine hydrochloride serves as a valuable intermediate in the asymmetric synthesis of biologically active compounds. By incorporating this compound into synthetic routes, chemists can access enantiopure molecules with enhanced therapeutic properties and reduced side effects. Additionally, (S)-6-Chlorochroman-4-amine hydrochloride can act as a key precursor for the development of novel materials and catalysts, further expanding its utility in organic chemistry applications.