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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)-

Acetic acid, [[(1S,2R,5S)-5-methyl-2-(1-methylethyl)cyclohexyl]oxy]-

C[C@H]1CC[C@@H]([C@H](C1)OCC(=O)O)C(C)C Request for Quotation
Chemical Name: Acetic acid, [[(1S,2R,5S)-5-methyl-2-(1-methylethyl)cyclohexyl]oxy]-
CAS Number: 94133-41-2
Product Number: AG003BD5(AGN-PC-0ONTFH)
Synonyms:
MDL No:
Molecular Formula: C12H22O3
Molecular Weight: 214.30128

Identification/Properties

Properties
Storage:
Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
214.305g/mol
XLogP3:
3.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
214.157g/mol
Monoisotopic Mass:
214.157g/mol
Topological Polar Surface Area:
46.5A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
213
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:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-[[(1S,2R,5S)-5-Methyl-2-(1-methylethyl)cyclohexyl]oxy]acetic acid is a versatile compound widely used in chemical synthesis for its unique properties and reactivity. In organic synthesis, this compound can serve as a key building block for the preparation of various complex molecules due to its functional groups and stereochemistry. It can be employed as a chiral auxiliary to induce stereo-specific reactions, allowing for the selective formation of enantiomerically pure products. Additionally, 2-[[(1S,2R,5S)-5-Methyl-2-(1-methylethyl)cyclohexyl]oxy]acetic acid can be utilized in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals where precise control over molecular structure and stereochemistry is crucial for desired activity and properties. Its applications extend to the creation of novel materials and the development of advanced synthetic methodologies in organic chemistry.