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  2. 2-[(1R,2R,5R)-5-methyl-2-propan-2-ylcyclohexyl]oxyacetyl chloride

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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)-

2-[(1R,2R,5R)-5-methyl-2-propan-2-ylcyclohexyl]oxyacetyl chloride

CC1CCC(C(C1)OCC(=O)Cl)C(C)C Request for Quotation
Chemical Name: 2-[(1R,2R,5R)-5-methyl-2-propan-2-ylcyclohexyl]oxyacetyl chloride
CAS Number: 15356-62-4
Product Number: AG0032AS(AGN-PC-094J2M)
Synonyms:
MDL No: MFCD00044947
Molecular Formula: C12H21ClO2
Molecular Weight: 232.7469

Identification/Properties

Computed Properties
Molecular Weight:
232.748g/mol
XLogP3:
4.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
4
Exact Mass:
232.123g/mol
Monoisotopic Mass:
232.123g/mol
Topological Polar Surface Area:
26.3A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
216
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

GHS Pictogram:
Signal Word:
Danger
UN#:
3265
Hazard Statements:
H314
Precautionary Statements:
P280-P305+P351+P338-P310
Class:
8
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


(-)-Menthoxyacetyl Chloride, a derivative of menthol, plays a crucial role in chemical synthesis as a versatile reagent. Its acyl chloride functional group enables it to be utilized in various reactions to introduce the menthoxyacetyl moiety into organic compounds. One common application of this compound is in the formation of esters through acylation reactions. In addition, (-)-Menthoxyacetyl Chloride can serve as a building block for the synthesis of complex molecules, such as pharmaceuticals and fragrances, due to its unique structure and reactivity. This reagent offers chemists the opportunity to incorporate the characteristic minty aroma and flavor of menthol into a wide range of products, making it a valuable tool in the field of organic chemistry.