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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)-

3-Buten-1-ol, 2-amino-, hydrochloride, (2S)-

N[C@@H](C=C)CO.Cl Request for Quotation
Chemical Name: 3-Buten-1-ol, 2-amino-, hydrochloride, (2S)-
CAS Number: 219803-57-3
Product Number: AG00BDFE(AGN-PC-0O7XEL)
Synonyms:
MDL No:
Molecular Formula: C4H10ClNO
Molecular Weight: 123.5813

Identification/Properties

Computed Properties
Molecular Weight:
123.58g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
123.045g/mol
Monoisotopic Mass:
123.045g/mol
Topological Polar Surface Area:
46.2A^2
Heavy Atom Count:
7
Formal Charge:
0
Complexity:
44.8
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


(S)-2-Aminobut-3-en-1-ol hydrochloride is a versatile compound that finds wide applications in chemical synthesis, particularly in the production of chiral molecules. This compound is valued for its ability to serve as a key building block in the creation of complex organic molecules with specific stereochemistry. By leveraging the chiral nature of (S)-2-Aminobut-3-en-1-ol hydrochloride, chemists can efficiently introduce asymmetry into their target molecules, enabling the synthesis of enantiomerically pure compounds. This compound is commonly used in the pharmaceutical, agrochemical, and materials science industries to create new compounds with enhanced properties and biological activities. Through precise manipulation of the functional groups on (S)-2-Aminobut-3-en-1-ol hydrochloride, chemists can tailor the structure of the resulting molecules to achieve desired properties, making it a valuable tool in organic synthesis.