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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)-

tert-butyl 2,7-diazaspiro[3.5]nonane-2-carboxylate;hydrochloride

O=C(N1CC2(C1)CCNCC2)OC(C)(C)C.Cl Request for Quotation
Chemical Name: tert-butyl 2,7-diazaspiro[3.5]nonane-2-carboxylate;hydrochloride
CAS Number: 929302-18-1
Product Number: AG00GTZ2(AGN-PC-04RZID)
Synonyms:
MDL No:
Molecular Formula: C12H23ClN2O2
Molecular Weight: 262.7762

Identification/Properties

Computed Properties
Molecular Weight:
262.778g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
262.145g/mol
Monoisotopic Mass:
262.145g/mol
Topological Polar Surface Area:
41.6A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
269
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
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

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The tert-Butyl 2,7-diazaspiro[3.5]nonane-2-carboxylate hydrochloride is a versatile compound that finds extensive application in chemical synthesis processes. Its unique structural features make it a valuable building block for preparing a variety of complex organic molecules. In organic synthesis, it serves as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. Its spirocyclic structure imparts specific stereochemical and steric properties, which are crucial in controlling the reactivity and selectivity of various chemical reactions. Moreover, the tert-Butyl 2,7-diazaspiro[3.5]nonane-2-carboxylate hydrochloride can facilitate the formation of intricate molecular architectures by participating in key bond-forming reactions such as N-alkylations, amidations, and cyclizations. Its application in chemical synthesis allows for the efficient and streamlined construction of diverse molecular scaffolds with implications in drug discovery and material science.