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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)-

1,2-Propanediamine, dihydrochloride, (2R)-

NC[C@H](N)C.Cl.Cl Request for Quotation
Chemical Name: 1,2-Propanediamine, dihydrochloride, (2R)-
CAS Number: 19777-67-4
Product Number: AG002B0W(AGN-PC-0QPBMK)
Synonyms:
MDL No:
Molecular Formula: C3H12Cl2N2
Molecular Weight: 147.0468

Identification/Properties

Properties
MP:
241-244 °C(lit.)
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
147.043g/mol
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
146.038g/mol
Monoisotopic Mass:
146.038g/mol
Topological Polar Surface Area:
52A^2
Heavy Atom Count:
7
Formal Charge:
0
Complexity:
20.9
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:
3
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
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


(R)-(+)-1,2-Diaminopropane dihydrochloride is a valuable reagent widely used in chemical synthesis for its chiral properties. This compound serves as a key building block in the preparation of enantiopure compounds, particularly in the pharmaceutical and fine chemical industries. Its ability to impart chirality into molecules makes it a crucial tool in asymmetric synthesis, allowing chemists to access enantiomerically pure products with high selectivity. (R)-(+)-1,2-Diaminopropane dihydrochloride finds applications in the synthesis of pharmaceutical intermediates, agrochemicals, and other complex organic molecules where enantiomeric purity is essential for their biological activity or functional properties. Through its use in various reactions such as asymmetric reductions, reductive aminations, and catalytic transformations, this compound enables the efficient and selective synthesis of chiral compounds, contributing to advances in drug discovery and materials science.