Description

4-Aminocyclohexanecarboxylic acid (CAS No. 3685-25-4) is a high-purity cyclohexane derivative with the molecular formula C₇H₁₃NO₂. This compound, also known by its IUPAC name 4-aminocyclohexane-1-carboxylic acid, is a valuable building block in organic synthesis and pharmaceutical research. Available in both cis and trans isomeric forms, it features an amino group and a carboxylic acid functional group on the cyclohexane ring, enabling versatile reactivity. Ideal for peptide modification, chiral synthesis, and medicinal chemistry applications, this product is rigorously tested for purity and consistency. Suitable for researchers requiring precise structural control in their experiments.

Properties

• CAS Number: 3685-25-4
• Complexity: 128
• IUPAC Name: 4-aminocyclohexanecarboxylic acid
• InChI: InChI=1S/C7H13NO2/c8-6-3-1-5(2-4-6)7(9)10/h5-6H,1-4,8H2,(H,9,10)
• InChI Key: DRNGLYHKYPNTEA-UHFFFAOYSA-N
• Exact Mass: 143.094628657
• Molecular Formula: C7H13NO2
• Molecular Weight: 143.18
• SMILES: C1CC(CCC1C(=O)O)N
• Topological: 63.3
• Monoisotopic Mass: 143.094628657
• Synonyms: trans-4-Aminocyclohexanecarboxylic acid, 4-Aminocyclohexanecarboxylic acid, 4-aminocyclohexane-1-carboxylic acid, cis-4-Amino-1-cyclohexanecarboxylic acid, 57043-03-5, 605-807-7, 626-259-5, 675-055-2, cis-4-Aminocyclohexanecarboxylic acid, 3685-23-2, 3685-25-4, 1776-53-0, cis-4-Aminocyclohexane carboxylic acid, cyclohexanecarboxylic acid, 4-amino-, MFCD00191730, trans-4-Amino-cyclohexanecarboxylic acid, cis-4-Aminohexahydrobenzoic Acid, 4-Amino-cyclohexanecarboxylic acid, CYCLOHEXANECARBOXYLIC ACID, 4-AMINO-, TRANS-, MFCD00191601, (1s,4s)-4-aminocyclohexane-1-carboxylic acid, MFCD00209953, 4-azanylcyclohexane-1-carboxylic acid, (1S,4S)-4-AMINOCYCLOHEXANECARBOXYLIC ACID, (1r,4r)-4-aminocyclohexanecarboxylic acid, trans-4-aminocyclohexane carboxylic acid, 4-Aminohexahydrobenzoic Acid, 4-aminocyclohexylcarboxylic acid, Cyclohexanecarboxylic acid, 4-amino-, cis-, cis-4-aminocyclohexanecarboxylicacid, (1r,4r)-4-aminocyclohexane-1-carboxylic acid, 4-Amino-1-carboxycyclohexane, (cis-4-Carboxycyclohexyl)amine, 3085-23-2, cis-4-amino-cyclohexanecarboxylic acid, NoName_367, 4-AMINOCYCLOHEXANE CARBOXYLIC ACID, UK 22314, (+-)-cis-4-Aminocyclohexanecarboxylic acid, 1,4-CIS-AMINOCYCLOHEXANECARBOXYLIC ACID, Oprea1_021616, 88456-98-8, SCHEMBL218064, SCHEMBL382975, SCHEMBL384165, SCHEMBL6986810, SCHEMBL6995757, DTXSID30901273, 4-amino cyclohexanecarboxylic acid, 4-aminocyclohexane-carboxylic acid, DRNGLYHKYPNTEA-IZLXSQMJSA-N, DRNGLYHKYPNTEA-OLQVQODUSA-N, BCP17255, BCP19613, BCP26653, cis-4-aminocyclohexylcarboxylic acid, NSC12784, NSC12785, STR06482, 4-amino-1-cyclohexanecarboxylic acid, NSC 12784, NSC 12785, NSC-12784, NSC-12785, SBB028269, STK724071, cis-4-Aminocyclohexyl carboxylic acid, trans-4-Aminocyclohexylcarboxylic acid, 4-amino-cyclohexane-1-carboxylic acid, AKOS004120822, AKOS005259585, AKOS006341988, cis-4-amino cyclohexyl carboxylic acid, cis-4-aminocyclohexane-carboxylic acid, cis-aminocyclohexane-4-carboxylic acid, CS-W005514, CS-W008392, CS-W016414, PB10129, PB21681, trans 4-amino-cyclohexanecarboxylic acid, cis-4-aminocyclohexane-1-carboxylic acid, (trans)-4-aminocyclohexanecarboxylic acid, BP-12344, DS-11045, DS-13960, SY002609, SY029216, SY038982, cis-4-amino-1-cyclohexane carboxylic acid, cis-4-Aminocyclohexanecarboxylic acid, 95%, DB-002973, DB-044306, DB-349170, A1278, A1656, ST50307499, 4-Aminocyclohexanecarboxylic acid, AldrichCPR, EN300-48596, EN300-86278, EN300-135332, trans-4-Aminocyclohexanecarboxylic acid, AldrichCPR, Q27456527, (cis-4-Carboxycyclohexyl)amine; (+/-)-cis-4-Aminocyclohexanecarboxylic Acid; 1,4-cis-Aminocyclohexanecarboxylic Acid; UK 22314; cis-4-Aminocyclohexane-1-carboxylic Acid

Application

4-Aminocyclohexanecarboxylic acid is widely used as a chiral scaffold in asymmetric synthesis and pharmaceutical intermediates. Its rigid cyclohexane backbone makes it valuable for conformational studies in peptide mimetics and bioactive molecule design. Researchers utilize this compound to explore structure-activity relationships in drug discovery, particularly in CNS-targeting compounds. It also serves as a precursor for functionalized cyclohexane derivatives in material science applications.

Safety and Hazards

GHS Hazard Statements

• H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]
• H319 (100%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]
• H335 (100%): May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation]

Precautionary Statements

• P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501

Hazard Classes and Categories

• Acute Tox. 4 (33.3%)
• Skin Irrit. 2 (100%)
• Eye Dam. 1 (33.3%)
• Eye Irrit. 2 (66.7%)
• STOT SE 3 (100%)

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