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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)-

Ternatin (peptide)

CC[C@@H]([C@H]1NC(=O)[C@H](NC(=O)[C@@H](C)N(C)C(=O)[C@H](C)N(C(=O)[C@@H](NC(=O)[C@@H](N(C(=O)[C@@H](N(C1=O)C)C)C)CC(C)C)CC(C)C)C)[C@@H](C(C)C)O)C Request for Quotation
Chemical Name: Ternatin (peptide)
CAS Number: 148619-41-4
Product Number: AG001L3J(AGN-PC-0Q2426)
Synonyms:
MDL No:
Molecular Formula: C37H67N7O8
Molecular Weight: 737.9700

Identification/Properties

Computed Properties
Molecular Weight:
737.984g/mol
XLogP3:
3.8
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
8
Rotatable Bond Count:
8
Exact Mass:
737.505g/mol
Monoisotopic Mass:
737.505g/mol
Topological Polar Surface Area:
189A^2
Heavy Atom Count:
52
Formal Charge:
0
Complexity:
1290
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
9
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


(2S)-1-phenylpropan-2-aminium chloride, also known as phenylpropanolamine hydrochloride, plays a crucial role in chemical synthesis as a versatile organic compound. This compound is commonly used as a chiral auxiliary in asymmetric synthesis, allowing for the creation of enantiomerically pure compounds. Its unique structural properties make it a valuable tool in the production of pharmaceuticals, agrochemicals, and other fine chemicals. Furthermore, (2S)-1-phenylpropan-2-aminium chloride serves as a key intermediate in the synthesis of various bioactive molecules, making it an essential component in the development of new drugs and chemical entities. Its ability to facilitate stereoselective reactions makes it a sought-after reagent in the field of synthetic organic chemistry.