Cas no 89115-95-7 ((2S)-2-methylpiperidine-2-carboxylic acid)

(2S)-2-methylpiperidine-2-carboxylic acid structure
89115-95-7 structure
Product Name:(2S)-2-methylpiperidine-2-carboxylic acid
CAS No:89115-95-7
MF:C7H13NO2
MW:143.183622121811
MDL:MFCD18207175
CID:711065
Update Time:2025-08-03

(2S)-2-methylpiperidine-2-carboxylic acid Chemical and Physical Properties

Names and Identifiers

    • (S)-2-Methylpiperidine-2-carboxylic acid
    • 2-Piperidinecarboxylicacid, 2-methyl-, (2S)-
    • 2-PIPERIDINECARBOXYLICACID,2-METHYL-,(2S)
    • 2-Piperidinecarboxylicacid,2-methyl-,(2S)-(9CI)
    • (2S)-2-METHYLPIPERIDINE-2-CARBOXYLIC ACID
    • 2973AH
    • SB13544
    • (S)-2-methylpiperidine-2-carboxylicacid
    • 2-Methylpiperidine-2alpha-carboxylic acid
    • (2S)-2-Methyl-2-piperidinecarboxylic acid (ACI)
    • 2-Piperidinecarboxylic acid, 2-methyl-, (S)- (ZCI)
    • (S)-2-Pipecoline-2-carboxylic acid
    • (2S)-2-methylpiperidine-2-carboxylic acid
    • MDL: MFCD18207175
    • Inchi: 1S/C7H13NO2/c1-7(6(9)10)4-2-3-5-8-7/h8H,2-5H2,1H3,(H,9,10)/t7-/m0/s1
    • InChI Key: GLNOAERYNWZGJY-ZETCQYMHSA-N
    • SMILES: C([C@@]1(CCCCN1[H])C)(O[H])=O

Computed Properties

  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 1
  • Complexity: 147
  • Topological Polar Surface Area: 49.3

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(2S)-2-methylpiperidine-2-carboxylic acid Production Method

Production Method 1

Reaction Conditions
1.1 Reagents: Hydrogen Catalysts: Palladium dihydroxide Solvents: Methanol ,  Water ;  24 h, 5 bar, rt
Reference
An efficient, asymmetric synthesis of pipecolic acid and 2-alkyl pipecolic acids
Hou, Duen-Ren; Hung, Shin-Yi; Hu, Chung-Cheng, Tetrahedron: Asymmetry, 2005, 16(23), 3858-3864

Production Method 2

Reaction Conditions
Reference
Synthesis and resolution of substituted pipecolic acids
Overberger, C. G.; Shalati, M. D., European Polymer Journal, 1983, 19(10-11), 1055-65

Production Method 3

Reaction Conditions
1.1 Reagents: Trimethylsilyl iodide Solvents: Chloroform
Reference
New synthetic method of optically active α-methylproline and α-methylpipecolinic acid using electrochemical oxidation as a key reaction
Matsumura, Yoshihiro; Kinoshita, Toshio; Yanagihara, Yuka; Kanemoto, Noriko; Watanabe, Mitsuaki, Tetrahedron Letters, 1996, 37(46), 8395-8398

(2S)-2-methylpiperidine-2-carboxylic acid Raw materials

(2S)-2-methylpiperidine-2-carboxylic acid Preparation Products

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