875798-79-1 (3-(4-AMINO-PHENYL)-PIPERIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER)

875798-79-1 (3-(4-AMINO-PHENYL)-PIPERIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER) Manufacturers in Hyderabad, India

Overview & Chemical Identity

CAS Number: 875798-79-1

Chemical Name: (3-(4-Aminophenyl)piperidine-1-carboxylic acid tert-butyl ester)

IUPAC Name: tert-Butyl 3-(4-aminophenyl)piperidine-1-carboxylate

Synonyms:
3-(4-Aminophenyl)-1-Boc-piperidine
tert-Butyl 3-(4-aminophenyl)piperidine-1-carboxylate
Boc-3-(4-aminophenyl)piperidine
(3-(4-Aminophenyl)piperidin-1-yl) tert-butyl carbonate

Molecular Formula: C₁₆H₂₄N₂O₂

Molecular Weight: ~276.38 g/mol


Physical & Chemical Properties

Appearance: White to off-white crystalline powder

Physical State: Solid

Melting Point: Typically 100–120 °C (may vary depending on purity and source)

Boiling Point: Not applicable (decomposes under high temperature)

Solubility:
Soluble in common organic solvents such as methanol, ethanol, ethyl acetate, dichloromethane (DCM), and DMSO; limited solubility in water

Stability:
Stable under normal laboratory conditions; sensitive to strong acids (Boc group cleavage) and strong oxidizing agents


Structural & Molecular Identifiers

Functional Groups:

  • Aromatic amine (–NH₂)

  • Piperidine ring

  • tert-Butyl ester (Boc protecting group)

  • Carbamate linkage (–NH–COO–)

  • Aromatic benzene ring

Chemical Class:
Protected amine / Carbamate derivative / Piperidine derivative

SMILES (representative):
CC(C)(C)OC(=O)N1CCC(CC1)C2=CC=C(C=C2)N

InChI Key (representative):
(Varies by database; available from chemical registries)


Functionality & Applications

Pharmaceutical Intermediate

875798-79-1 is commonly used as a protected piperidine building block in pharmaceutical synthesis. The tert-butyl carbamate (Boc) group protects the nitrogen atom during multi-step synthetic processes.

It is particularly valuable for:

  • Construction of heterocyclic drug candidates

  • Development of CNS-active molecules

  • Preparation of kinase inhibitors and receptor-targeting compounds


Fine Chemical & Medicinal Chemistry Applications

  • Intermediate for biologically active compounds

  • Building block for SAR (Structure–Activity Relationship) studies

  • Precursor for amine-functionalized derivatives after Boc deprotection

  • Used in combinatorial chemistry and lead optimization programs

The presence of both an aromatic amine and a protected piperidine makes it highly versatile for further derivatization.


Research & Development

Commonly employed in:

  • Academic synthetic organic chemistry

  • Medicinal chemistry research

  • Drug discovery programs

  • Multi-step synthesis of advanced intermediates

The Boc protecting group allows selective deprotection under acidic conditions, enabling controlled synthetic transformations.


Safety & Handling

GHS Classification (typical for similar compounds):

  • Harmful if swallowed

  • Causes skin and eye irritation

  • May cause respiratory irritation

Common Hazard Statements:

  • H302: Harmful if swallowed

  • H315: Causes skin irritation

  • H319: Causes serious eye irritation

  • H335: May cause respiratory irritation

Precautionary Statements:

  • P261: Avoid breathing dust

  • P280: Wear protective gloves and eye protection

  • P305 + P351 + P338: IF IN EYES, rinse cautiously with water and remove contact lenses

  • P301 + P312: IF SWALLOWED, call a doctor if you feel unwell

Handle in a well-ventilated laboratory using appropriate personal protective equipment (PPE).


Practical Details & Supplier Information

Typical Purity: 97–99% (Research and Industrial Grade)

Storage Conditions:

  • Store in a tightly sealed container

  • Keep in a cool, dry, and well-ventilated area

  • Protect from moisture and direct sunlight

  • Avoid strong acids and oxidizing agents

Commercial Use:
Supplied by specialty chemical manufacturers for research and industrial organic synthesis.
Not intended for direct pharmaceutical, food, or diagnostic use without proper regulatory compliance.


Summary Statement

875798-79-1 (3-(4-AMINO-PHENYL)-PIPERIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER) is a versatile protected piperidine derivative widely used as a pharmaceutical intermediate. Its combination of an aromatic amine functionality and Boc-protected nitrogen makes it an essential building block in medicinal chemistry, fine chemical synthesis, and advanced organic research applications.

As a trusted manufacturer and supplier in Hyderabad, SriniChem provides high-quality 875798-79-1 (3-(4-AMINO-PHENYL)-PIPERIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER) produced under strict quality control standards. Our product, with CAS No: 875798-79-1, is suitable for both research and industrial use. Choose SriniChem for reliable supply, technical expertise, and customer-focused service. Contact SriniChem today for 3-(4-AMINO-PHENYL)-PIPERIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER.