Atomfair N-[2,6-Bis(1-methylethyl)-4-phenoxyphenyl]thiourea C19H24N2OS CAS 135252-10-7

Description

N-[2,6-Bis(1-methylethyl)-4-phenoxyphenyl]thiourea (CAS No. 135252-10-7) is a high-purity thiourea derivative with the molecular formula C₁₉H₂₄N₂OS. This compound features a sterically hindered phenyl ring substituted with two isopropyl groups and a phenoxy moiety, making it a valuable intermediate in organic synthesis and pharmaceutical research. Its IUPAC name is [4-phenoxy-2,6-di(propan-2-yl)phenyl]thiourea, and it is characterized by its thiourea functional group, which is widely utilized in metal coordination chemistry and as a precursor for heterocyclic compounds. Suitable for researchers and scientists, this product is rigorously tested for purity and stability, ensuring reliable performance in advanced chemical applications.

Properties

• CAS Number: 135252-10-7
• Complexity: 362
• IUPAC Name: (2,6-diisopropyl-4-phenoxy-phenyl)thiourea
• InChI: InChI=1S/C19H24N2OS/c1-12(2)16-10-15(22-14-8-6-5-7-9-14)11-17(13(3)4)18(16)21-19(20)23/h5-13H,1-4H3,(H3,20,21,23)
• InChI Key: RBDFBEPKVUICAS-UHFFFAOYSA-N
• Exact Mass: 328.16093457
• Molecular Formula: C19H24N2OS
• Molecular Weight: 328.5
• SMILES: CC(C)C1=CC(=CC(=C1NC(=S)N)C(C)C)OC2=CC=CC=C2
• Topological: 79.4
• Monoisotopic Mass: 328.16093457
• Synonyms: 135252-10-7, N-[2,6-Bis(1-methylethyl)-4-phenoxyphenyl]thiourea, N-(2,6-Bis(1-methylethyl)-4-phenoxyphenyl)thiourea, (2,6-Diisopropyl-4-Phenoxy)Phenylthiourea, N-(4-phenoxy-2,6-diisopropylphenyl)thiourea, [4-phenoxy-2,6-di(propan-2-yl)phenyl]thiourea, 4-Phenoxy-2,6-diisopropyl phenyl thiourea, (2,6-diisopropyl-4-phenoxy-phenyl)thioure, SCHEMBL9780906, DTXSID401226419, AKOS015909584, (2 pound not6-Diisopropyl-4-Phenoxy)Phenylthiourea, Thiourea, N-[2,6-bis(1-methylethyl)-4-phenoxyphenyl]-

Application

N-[2,6-Bis(1-methylethyl)-4-phenoxyphenyl]thiourea is primarily used as a key intermediate in the synthesis of bioactive molecules and pharmaceutical agents. Its thiourea moiety makes it a versatile ligand in coordination chemistry, particularly for transition metal complexes. Researchers also employ this compound in the development of novel heterocyclic frameworks due to its sterically hindered aromatic core. Additionally, it may serve as a precursor for agrochemicals or specialty polymers requiring tailored steric and electronic properties.

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