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线性分子式:
CH3CH=CHCH=CHCHO
化学文摘社编号:
分子量:
96.13
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
205-564-3
Beilstein/REAXYS Number:
1698401
MDL number:
产品名称
(E,E)-2,4-己二烯醛, 95%
InChI key
BATOPAZDIZEVQF-MQQKCMAXSA-N
InChI
1S/C6H8O/c1-2-3-4-5-6-7/h2-6H,1H3/b3-2+,5-4+
SMILES string
[H]C(=O)\C=C\C=C\C
vapor density
>1 (vs air)
assay
95%
form
liquid
refractive index
n20/D 1.541 (lit.)
bp
69 °C/20 mmHg (lit.)
density
0.895 g/mL at 20 °C
0.871 g/mL at 25 °C (lit.)
functional group
aldehyde
storage temp.
2-8°C
Quality Level
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Application
反式,反式-2,4-己二醛(山梨醛)用于合成手性环加合物。
General description
反,反-2,4-己二烯醛是一种α,β-不饱和醛,可用作食品添加和各种化学和制药行业中的起始原料。
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Eye Dam. 1 - Skin Corr. 1B - Skin Sens. 1
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
flash_point_f
154.0 °F - closed cup
flash_point_c
67.77 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Atmospheric reactions between E, E-2, 4-hexadienal and OH, NO3 radicals and Cl atoms
Colmenar, et al.
Atmospheric Environment, 99, 159-167 (2014)
De novo asymmetric synthesis of two 5-amino-5, 6-dideoxy-D-allose derivatives.
Tetrahedron Letters, 35(31), 5653-5656 (1994)
Influence of 1-butanethiol and metal ions on hydrogenation of trans, trans-2, 4-hexadienal at platinum nanocatalysts
Du, YK and Xu, et al.
Colloids and Surfaces. A, Physicochemical and Engineering Aspects, 257, 75-78 (2005)
Margaret P O'Connor et al.
Physical chemistry chemical physics : PCCP, 8(44), 5236-5246 (2007-01-05)
The atmospheric photolysis of E-2-hexenal, Z-3-hexenal and E,E-2,4-hexadienal has been investigated at the large outdoor European Photoreactor (EUPHORE) in Valencia, Spain. E-2-Hexenal and E,E-2,4-hexadienal were found to undergo rapid isomerization to produce Z-2-hexenal and a ketene-type compound (probably E-hexa-1,3-dien-1-one), respectively.
exo-Selective asymmetric Diels-Alder reaction of 2,4-dienals and nitroalkenes by trienamine catalysis.
Zhi-Jun Jia et al.
Angewandte Chemie (International ed. in English), 50(37), 8638-8641 (2011-07-26)
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