10-UNDECEN-1-OL - CAS 112-43-6
Category:
Flavor & Fragrance
Product Name:
10-UNDECEN-1-OL
Synonyms:
10-UNDECEN-1-OL, 10-Undecenol, Alcohol C-11, undecylenic, Undecen-1-ol, Undecylenyl alcohol, 10-UNDECEN-1-OL NO ANTIOXIDANT (special order)
CAS Number:
112-43-6
Molecular Weight:
170.29
Molecular Formula:
C11H22O
COA:
Inquire
MSDS:
Inquire
Olfactive Family:
Floral | Waxy
Odor description:
A pleasant soapy, waxy, floral, rose aroma.
Chemical Structure
CAS 112-43-6 10-UNDECEN-1-OL

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Reference Reading


1.Novel vanadium(III) complexes with bidentate N,N-chelating iminopyrrolide ligands: synthesis, characterization and catalytic behaviour of ethylene polymerization and copolymerization with 10-undecen-1-ol.
Xu BC1, Hu T, Wu JQ, Hu NH, Li YS. Dalton Trans. 2009 Nov 7;(41):8854-63. doi: 10.1039/b909495d. Epub 2009 Sep 7.
A series of novel vanadium(III) complexes bearing iminopyrrolide chelating ligands [2-(RN=CH)C4H3N]V(THF)2Cl2 (2a: R = cyclohexyl; 2b: R = Ph; 2c: R = 2,6-iPr2C6H3; 2d: R = p-CF3C6H4; 2e: R = C6F5) have been synthesized and characterized. Single-crystal X-ray diffraction revealed that complexes 2a, 2c and 2e adopt an octahedral geometry around the vanadium center. In the presence of Et2AlCl as a co-catalyst, these complexes displayed high catalytic activities up to 48.6 kg PE mmol(V)(-1) h(-1) bar(-1) for ethylene polymerization, and produced high molecular weight polymers. 2a-e/Et2AlCl catalytic systems were tolerant to elevated temperature (70 degrees C) and yielded unimodal polyethylenes, indicating the single site behaviour of these catalysts. By pre-treating with equimolar amounts of alkylaluminums, functional alpha-olefin 10-undecen-1-ol can be efficiently incorporated into polyethylene chains. 10-Undecen-1-ol incorporation can easily reach 15.
2.A facile synthesis of the sex pheromone of the red bollworm moth from 10-undecen-1-ol.
Babler JH, Martin MJ. J Org Chem. 1977 May 13;42(10):1799-1800.