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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)-

4-METHOXYCARBONYL-BICYCLO[2.2.2]OCT-1-YL AMMONIUM CHLORIDE

COC(=O)C12CCC(CC1)(CC2)N.Cl Request for Quotation
Chemical Name: 4-METHOXYCARBONYL-BICYCLO[2.2.2]OCT-1-YL AMMONIUM CHLORIDE
CAS Number: 135908-43-9
Product Number: AG0080DV(AGN-PC-09T1XF)
Synonyms:
MDL No:
Molecular Formula: C10H18ClNO2
Molecular Weight: 219.7084

Identification/Properties

Computed Properties
Molecular Weight:
219.709g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
219.103g/mol
Monoisotopic Mass:
219.103g/mol
Topological Polar Surface Area:
52.3A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
213
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


Bicyclo[2.2.2]octane-1-carboxylic acid, 4-amino-, methyl ester, hydrochloride (1:1) is a versatile compound that finds application in various chemical synthesis reactions. This compound is commonly used as a building block in the synthesis of pharmaceutical intermediates and agrochemicals. Its unique molecular structure imparts specific reactivity in certain chemical reactions, making it a valuable tool for the creation of complex molecules. Additionally, the hydrochloride salt form of this compound enhances its solubility in polar solvents, further expanding its utility in synthetic chemistry. Whether employed as a precursor for the preparation of novel compounds or as a key reactant in multistep synthetic pathways, Bicyclo[2.2.2]octane-1-carboxylic acid, 4-amino-, methyl ester, hydrochloride (1:1) offers exciting opportunities for advancing the field of chemical synthesis.