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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)-

(R)-3-Aminotetrahydropyran Hydrochloride

N[C@@H]1CCCOC1.Cl Request for Quotation
Chemical Name: (R)-3-Aminotetrahydropyran Hydrochloride
CAS Number: 1315500-31-2
Product Number: AG000ZED(AGN-PC-0WA2MN)
Synonyms:
MDL No: MFCD09056863
Molecular Formula: C5H12ClNO
Molecular Weight: 137.6079

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
137.607g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
137.061g/mol
Monoisotopic Mass:
137.061g/mol
Topological Polar Surface Area:
35.2A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
56
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-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


(R)-Tetrahydro-2H-pyran-3-amine hydrochloride is a versatile compound widely used in chemical synthesis for its unique properties. This compound serves as a valuable chiral building block in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Due to its asymmetric structure, (R)-Tetrahydro-2H-pyran-3-amine hydrochloride can be utilized in asymmetric synthesis to introduce chirality into various organic molecules. Its presence in the synthesis of complex organic compounds enhances the overall stereochemical control, leading to the production of enantiomerically pure substances. In addition to its application in chiral synthesis, this compound also acts as a key intermediate in the preparation of bioactive compounds and functional materials. With its significant role in chemical synthesis, (R)-Tetrahydro-2H-pyran-3-amine hydrochloride contributes to the advancement of diverse fields within the chemical industry.