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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)-

(S)-2-Azido Isovaleric Acid Cyclohexylammonium Salt

NC1CCCCC1.[N-]=[N+]=N[C@H](C(=O)O)C(C)C Request for Quotation
Chemical Name: (S)-2-Azido Isovaleric Acid Cyclohexylammonium Salt
CAS Number: 1217462-63-9
Product Number: AG0015OK(AGN-PC-0WAFV0)
Synonyms:
MDL No:
Molecular Formula: C11H22N4O2
Molecular Weight: 242.3180

Identification/Properties

Properties
MP:
121-123°C
Storage:
-10 ℃;Light sensitive;
Form:
Solid
Computed Properties
Molecular Weight:
242.323g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
3
Exact Mass:
242.174g/mol
Monoisotopic Mass:
242.174g/mol
Topological Polar Surface Area:
77.7A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
218
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-Azido Isovaleric Acid Cyclohexylammonium Salt is a versatile compound commonly used in chemical synthesis as a key building block. It serves as a valuable precursor in the preparation of various azido-containing compounds, which are essential intermediates in the synthesis of pharmaceuticals, agrochemicals, and materials. This compound's unique structure and reactivity make it particularly useful in click chemistry reactions, where it participates in azide-alkyne cycloadditions to form triazole linkages efficiently. Additionally, (S)-2-Azido Isovaleric Acid Cyclohexylammonium Salt can be employed in the modification of biomolecules, polymer functionalization, and the synthesis of complex organic molecules. Its application in chemical synthesis offers chemists a powerful tool for constructing diverse molecular architectures with high precision and efficiency.