Chnnamyl alcohol – 98%, high purity , CAS No.104-54-1

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Sku: 1759800656-2958
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Pubchem Sid488195330 Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488195330 Canonical SmilesC1=CC=C(C=C1)C=CCO IUPAC Name(E)-3-phenylprop-2-en-1-ol InChIKeyOOCCDEMITAIZTP-QPJJXVBHSA-N INCHI1S/C9H10O/c10-8-4-7-9-5-2-1-3-6-9/h1-7,10H,8H2/b7-4+ Isomeric SMILES C1=CC=C(C=C1)/C=C/CO WGK Germany 2 RTECS GE2200000 Alternate CAS 4407-36-7 UN Number 1987 Molecular Weight 134.18 Beilstein 1903999 Reaxy-Rn 1903999 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1903999&ln=
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Description

Cinnamyl alcohol causes Friedel Crafts alkylation of bulky aromatic compound 2,4-di-tert-butylphenol using mesoporous aluminosilicate as catalyst. Cinnamyl alcohol undergoes partial oxidation in air to form cinnamaldehyde over a series of Bi-Pt/alumina catalysts. Cinnamyl alcohol is used in perfumery and in deodorant compositions.
Cinnamyl alcohol was used to study the alkylation of 2,4-di-tert-butylphenol by cinnamyl alcohol using aluminum-containing mesoporous ethane-silica catalyst. It was used to study gold nanoparticles supported on titanium dioxide catalysed oxidative coupling of alcohols and amines to form the corresponding imines.

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