46188
法尼醛，异构体混合物
technical
别名:
3,7,11-三甲基-2,6,10-十二烷三烯醛
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关于此项目
经验公式（希尔记法）:
C15H24O
化学文摘社编号:
分子量:
220.35
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
242-957-9
Beilstein/REAXYS Number:
1723427
MDL number:
产品名称
法尼醛，异构体混合物, technical
InChI key
YHRUHBBTQZKMEX-YFVJMOTDSA-N
InChI
1S/C15H24O/c1-13(2)7-5-8-14(3)9-6-10-15(4)11-12-16/h7,9,11-12H,5-6,8,10H2,1-4H3/b14-9+,15-11+
SMILES string
[H]C(=O)\C=C(/C)CC\C=C(/C)CC\C=C(/C)C
grade
technical
impurities
≤3% water
refractive index
n20/D >1.4920 (lit.)
n20/D 1.497
bp
126-129 °C/3.5 mmHg (lit.)
density
0.909 g/mL at 25 °C (lit.)
functional group
aldehyde
Quality Level
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Application
法呢醛用于倍半萜烯纳纳莫尔的合成。
General description
据报告，法呢醛是醛酮还原酶1B10（AKR1B10）的特异性脂质底物。法呢醇与布朗葡萄藻B种族菌株的原生质体一起培养导致法呢醛和3-羟基-2，3-二氢法呢醛的形成。
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
10 - Combustible liquids
wgk
WGK 2
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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Experimental & applied acarology, 29(3-4), 279-291 (2003-11-26)
The composition of oil gland exudates from two oribatid mites, Trhypochthoniellus sp. and Trhypochthonius japonicus, was studied with reference to the related species Trhypochthoniellus crassus. Trhypochthoniellus sp. contained a mixture of seven compounds; (Z,Z)-6,9-heptadecadiene, geranial, 3-hydroxybenzene-1,2-dicarbaldehyde (gamma-acaridial), neryl formate, neral
Kenji Shimomura et al.
Journal of chemical ecology, 34(4), 467-477 (2008-03-21)
The southern cowpea weevil, Callosobruchus chinensis (Coleoptera: Bruchidae), is a major pest of stored legumes in warm temperate and tropical climates. The female sex attractant pheromone was extracted from filter-paper shelters taken from containers that housed virgin females. The extracts
W R Tschantz et al.
The Journal of biological chemistry, 276(4), 2321-2324 (2000-11-18)
Prenylated proteins contain either a 15-carbon farnesyl or a 20-carbon geranylgeranyl isoprenoid covalently attached via a thioether bond to a cysteine residue at or near their C terminus. As prenylated proteins comprise up to 2% of the total protein in
Constantinos Tsangarakis et al.
The Journal of organic chemistry, 73(7), 2905-2908 (2008-03-07)
The sesquiterpene nanaimoal was synthesized in 21% overall yield and in a biomimetic manner. As a key step, the acid-catalyzed cyclization of farnesal under zeolite NaY confinement conditions was used. The intrazeolite cyclization of farnesal affords as major product a
Grace Jones et al.
The FEBS journal, 273(21), 4983-4996 (2006-10-27)
The in vivo ligand-binding function and ligand-binding activity of the Drosophila melanogaster retinoid-X receptor (RXR) ortholog, ultraspiracle, toward natural farnesoid products of the ring gland were assessed. Using an equilibrium fluorescence-binding assay, farnesoid products in the juvenile hormone (JH) biosynthesis
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