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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 ((1R,2S,5S)-2-amino-5-(dimethylcarbamoyl)cyclohexyl)carbamate oxalate

OC(=O)C(=O)O.O=C(OC(C)(C)C)N[C@@H]1C[C@H](CC[C@@H]1N)C(=O)N(C)C Request for Quotation
Chemical Name: tert-Butyl ((1R,2S,5S)-2-amino-5-(dimethylcarbamoyl)cyclohexyl)carbamate oxalate
CAS Number: 1210348-34-7
Product Number: AG008TPM(AGN-PC-0WAM8N)
Synonyms:
MDL No:
Molecular Formula: C16H29N3O7
Molecular Weight: 375.4174

Identification/Properties

Computed Properties
Molecular Weight:
375.422g/mol
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
8
Rotatable Bond Count:
5
Exact Mass:
375.201g/mol
Monoisotopic Mass:
375.201g/mol
Topological Polar Surface Area:
159A^2
Heavy Atom Count:
26
Formal Charge:
0
Complexity:
435
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
3
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-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


The tert-Butyl ((1R,2S,5S)-2-amino-5-(dimethylcarbamoyl)cyclohexyl)carbamate oxalate is a crucial compound widely used in chemical synthesis for its unique properties and versatile applications. In organic synthesis, this compound serves as a valuable building block for the preparation of various complex molecules and pharmaceutical intermediates. It acts as a protecting group for the amino and carbamate functionalities, allowing for selective modifications during the synthesis process. Additionally, the oxalate moiety plays a pivotal role in facilitating reactions and enhancing the overall reactivity of the compound. Overall, tert-Butyl ((1R,2S,5S)-2-amino-5-(dimethylcarbamoyl)cyclohexyl)carbamate oxalate is a valuable tool in the hands of chemists, enabling efficient and precise control over chemical transformations and providing a pathway for the synthesis of diverse organic molecules.