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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)-

Cyclohexanepropanoic acid, a-amino-, methyl ester, hydrochloride

COC(=O)C(CC1CCCCC1)N.Cl Request for Quotation
Chemical Name: Cyclohexanepropanoic acid, a-amino-, methyl ester, hydrochloride
CAS Number: 144600-01-1
Product Number: AG001JTH(AGN-PC-0PVU1O)
Synonyms:
MDL No: MFCD00153486
Molecular Formula: C10H20ClNO2
Molecular Weight: 221.7243

Identification/Properties

Computed Properties
Molecular Weight:
221.725g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
221.118g/mol
Monoisotopic Mass:
221.118g/mol
Topological Polar Surface Area:
52.3A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
164
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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:
H317-H319
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


H-Cha-OMe.HCl, also known as hydroxylamine-O-methyl chloride, is a valuable reagent in chemical synthesis due to its versatility and unique properties. This compound is commonly used in organic chemistry for various reactions and transformations. Its primary application lies in the conversion of carbonyl compounds to oximes, a reaction known as oximation.In the process of oximation, H-Cha-OMe.HCl acts as a nucleophile, attacking the electrophilic carbon of the carbonyl group to form an oxime. This reaction is useful in the synthesis of various organic compounds, including pharmaceuticals, agrochemicals, and fragrances. Additionally, H-Cha-OMe.HCl can be employed in the modification of biomolecules and the preparation of heterocyclic compounds.Furthermore, H-Cha-OMe.HCl can also participate in rearrangement reactions and serve as a protecting group for carbonyl functionalities. Its ease of handling and compatibility with a wide range of solvents make it a convenient and reliable reagent for synthetic chemists. Overall, H-Cha-OMe.HCl plays a crucial role in the synthesis of complex organic molecules and is an essential tool in modern chemical research.