1. Home
  2. (2R,3R)-2-methyl-1-[(2-methylpropan-2-yl)oxycarbonyl]piperidine-3-carboxylic acid

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

(2R,3R)-2-methyl-1-[(2-methylpropan-2-yl)oxycarbonyl]piperidine-3-carboxylic acid

CC1N(CCCC1C(=O)[O-])C(=O)OC(C)(C)C Request for Quotation
Chemical Name: (2R,3R)-2-methyl-1-[(2-methylpropan-2-yl)oxycarbonyl]piperidine-3-carboxylic acid
CAS Number: 249762-01-4
Product Number: AG002Q1M(AGN-PC-040X9Q)
Synonyms:
MDL No:
Molecular Formula: C12H20NO4-
Molecular Weight: 242.2915

Identification/Properties

Computed Properties
Molecular Weight:
243.303g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
243.147g/mol
Monoisotopic Mass:
243.147g/mol
Topological Polar Surface Area:
66.8A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
308
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
2
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


The compound 1-(tert-Butoxycarbonyl)-2-methylpiperidine-3-carboxylic acid, also known as $name$, plays a crucial role in chemical synthesis as a versatile building block. This compound is commonly used as a protecting group in organic synthesis to temporarily shield the amine functionality of a molecule. By selectively blocking the amine group with the tert-butoxycarbonyl (Boc) moiety, chemists can prevent undesired reactions from occurring at this site while allowing other reactions to proceed. This protection strategy is particularly useful in multi-step synthesis processes where the amine group needs to be preserved for specific reactions, such as amidation or coupling reactions. Additionally, the Boc group can be easily removed under mild conditions, regenerating the free amine functionality and enabling the synthesis of complex molecules with high efficiency and precision. The application of 1-(tert-Butoxycarbonyl)-2-methylpiperidine-3-carboxylic acid in chemical synthesis highlights its importance as a valuable tool for controlling reactivity and achieving desired chemical transformations in a controlled manner.