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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)-

Ornithine,2-(difluoromethyl)-, hydrochloride, hydrate (1:1:1)

NCCCC(C(=O)O)(C(F)F)N.O.Cl Request for Quotation
Chemical Name: Ornithine,2-(difluoromethyl)-, hydrochloride, hydrate (1:1:1)
CAS Number: 96020-91-6
Product Number: AG005W0A(AGN-PC-0W5M6P)
Synonyms:
MDL No:
Molecular Formula: C6H15ClF2N2O3
Molecular Weight: 236.6447

Identification/Properties

Properties
MP:
>210°C (dec.)
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
236.644g/mol
Hydrogen Bond Donor Count:
5
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
5
Exact Mass:
236.074g/mol
Monoisotopic Mass:
236.074g/mol
Topological Polar Surface Area:
90.3A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
166
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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:
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


Ornithine, 2-(difluoromethyl)-, hydrochloride, hydrate (1:1:1) is a versatile compound that finds wide application in chemical synthesis. This compound serves as a valuable building block in organic chemistry, enabling the creation of complex molecules through various synthetic routes. By incorporating Ornithine, 2-(difluoromethyl)-, hydrochloride, hydrate (1:1:1) into reaction sequences, chemists can access new structural motifs and functional groups, expanding the scope of synthetic possibilities. Through its strategic use in chemical transformations, this compound contributes to the development of novel materials, pharmaceuticals, and agrochemicals, driving innovation in the field of chemistry.