CAS 625471-18-3

(S)-tert-Butyl 3-aminopiperidine-1-carboxylate

Description:

(S)-tert-Butyl 3-aminopiperidine-1-carboxylate is a chemical compound characterized by its piperidine ring structure, which is a six-membered saturated nitrogen-containing heterocycle. The compound features a tert-butyl group, providing steric bulk and hydrophobic characteristics, which can influence its solubility and reactivity. The presence of an amino group at the 3-position of the piperidine ring contributes to its potential as a building block in pharmaceutical synthesis, particularly in the development of biologically active molecules. The carboxylate functional group enhances its reactivity, allowing for various chemical transformations. This compound is typically used in organic synthesis and medicinal chemistry, where its stereochemistry (the (S) configuration) is crucial for biological activity. Additionally, its molecular properties, such as polarity and potential for hydrogen bonding, make it a versatile intermediate in the synthesis of more complex compounds. Safety and handling precautions should be observed, as with all chemical substances, to mitigate any risks associated with its use.

Formula: C₁₀H₂₀N₂O₂

InChI: InChI=1S/C10H20N2O2/c1-10(2,3)14-9(13)12-6-4-5-8(11)7-12/h8H,4-7,11H2,1-3H3/t8-/m0/s1

InChI key: InChIKey=AKQXKEBCONUWCL-QMMMGPOBSA-N

SMILES: C(OC(C)(C)C)(=O)N1C[C@@H](N)CCC1

Synonyms:

• (3S)-Aminopiperidine-1-carboxylic acid tert-butyl ester
• (S)-1-Boc-3-Aminopiperidine
• (S)-1-Boc-3-piperidinamine
• (S)-1-tert-Butoxycarbonyl-3-aminopiperidine
• (S)-3-Amino-1-(tert-butoxycarbonyl)piperidine
• (S)-3-Amino-1-Boc-Piperidine
• (S)-3-Aminopiperidine-1-carboxylic acid tert-butyl ester
• (S)-tert-Butyl 3-aminopiperidine-1-carboxylate
• (S)-tert-Butyl3-aminopiperidinecarboxylate
• 1,1-Dimethylethyl (3S)-3-aminopiperidine-1-carboxylate
• 1-Piperidinecarboxylic acid, 3-amino-, 1,1-dimethylethyl ester, (3S)-
• 3-Aminopiperidine-1-carboxylic acid (S)-tert-butyl ester
• S-1-N-Boc-3-Amino Piperidine
• tert-Butyl (S)-3-aminopiperidine-1-carboxylate
• tert-butyl (3S)-3-aminopiperidine-1-carboxylate

(S)-3-Amino-1-tert-butoxycarbonylpiperidine

CAS: 625471-18-3

Formula: C₁₀H₂₀N₂O₂

Purity: >95.0%(GC)(T)

Color and Shape: Light yellow to Yellow to Orange clear liquid

Molecular weight: 200.28

Ref: 3B-A2335

(S)-(+)-3-Amino-1-Boc-piperidine, 97%

CAS: 625471-18-3

(S)-(+)-3-Amino-1-Boc-piperidine is used to prepare selective noncovalent inhibitors of the bacterial cysteine protease IdeS. The product obtained by the reductive elimination reaction with ethylglyoxalte is used as a reference compound, which is used to determine the absolute configuration of the t

Formula: C₁₀H₂₀N₂O₂

Purity: 97%

Color and Shape: Liquid or viscous liquid, Clear colorless to yellow

Molecular weight: 200.28

Ref: 02-H30538

(S)-1-Boc-3-Aminopiperidine

CAS: 625471-18-3

Formula: C₁₀H₂₀N₂O₂

Purity: 97%

Color and Shape: Liquid

Molecular weight: 200.2780

Ref: IN-DA0032GH

(3S)-3-Aminopiperidine, N1-BOC protected

CAS: 625471-18-3

(3S)-3-Aminopiperidine, N1-BOC protected

Formula: C₁₀H₂₀N₂O₂

Purity: ≥95%

Color and Shape: clear. viscous. colourless liquid

Molecular weight: 200.28g/mol

Ref: 54-OR4588

(S)-tert-Butyl 3-Aminopiperidine-1-carboxylate

Controlled Product

CAS: 625471-18-3

Formula: C₁₀H₂₀N₂O₂

Color and Shape: Neat

Molecular weight: 200.28

Ref: TR-S960110

(S)-3-Amino-1-N-Boc-piperidine

CAS: 625471-18-3

Formula: C₁₀H₂₀N₂O₂

Purity: 97%

Color and Shape: Oil

Molecular weight: 200.282

Ref: 10-F011309