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About This Item
经验公式（希尔记法）:
C15H24O
CAS号:
分子量:
220.35
Beilstein:
1723427
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22
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等級
technical
品質等級
雜質
≤3% water
折射率
n20/D >1.4920 (lit.)
n20/D 1.497
bp
126-129 °C/3.5 mmHg (lit.)
密度
0.909 g/mL at 25 °C (lit.)
官能基
aldehyde
SMILES 字串
[H]C(=O)\C=C(/C)CC\C=C(/C)CC\C=C(/C)C
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+
InChI 密鑰
YHRUHBBTQZKMEX-YFVJMOTDSA-N
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一般說明
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。
應用
法呢醛用于倍半萜烯纳纳莫尔的合成。
訊號詞
Warning
危險聲明
危險分類
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
10 - Combustible liquids
水污染物質分類（WGK）
WGK 2
閃點（°F）
235.4 °F - closed cup
閃點（°C）
113 °C - closed cup
個人防護裝備
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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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
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A human aldose reductase-like protein, AKR1B10 in the aldo-keto reductase (AKR) superfamily, was recently identified as a therapeutic target in the treatment of several types of cancer. In order to identify potential leads for new inhibitors of AKR1B10, we adopted
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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
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Journal of chemical ecology, 36(8), 824-833 (2010-07-08)
Callosobruchus rhodesianus (Pic) (Coleoptera: Chrysomelidae: Bruchinae) is a pest of stored legumes through the Afro-tropical region. In laboratory bioassays, males of C. rhodesianus were attracted to volatiles collected from virgin females. Collections were purified by various chromatographic techniques, and the
H Inoue et al.
Biochemical and biophysical research communications, 196(3), 1401-1405 (1993-11-15)
Farnesal and 3-hydroxy-2,3-dihydrofarnesal (3-hydroxy-3,7,11-trimethyl-6,10-dodecadiene-1-al) were formed from farnesol when the alcohol was incubated with the protoplast of Botryococcus braunii B race strain. This fact suggests the existence of farnesal hydratase in the alga. Feeding experiments showed that both farnesal and
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