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折射率
n20/D 1.448 (lit.)
密度
0.878 g/mL at 25 °C (lit.)
官能基
allyl
hydroxyl
SMILES 字串
OC(CC=C)C=C
InChI
1S/C6H10O/c1-3-5-6(7)4-2/h3-4,6-7H,1-2,5H2
InChI 密鑰
SZYLTIUVWARXOO-UHFFFAOYSA-N
一般說明
1,5-Hexadien-3-ol is the starting reagent for the enantioselective synthesis of (+)-rogioloxepane A. It undergoes Sharpless kinetic resolution and ring-closing metathesis to yield nine membered oxocene.
應用
1,5-Hexadien-3-ol was used in the synthesis of (+)-obtusenyne.
訊號詞
Warning
危險聲明
危險分類
Flam. Liq. 3
儲存類別代碼
3 - Flammable liquids
水污染物質分類(WGK)
WGK 3
閃點(°F)
84.2 °F - closed cup
閃點(°C)
29 °C - closed cup
個人防護裝備
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Induction of rejection of successful allografts of rat islets by donor peritoneal exudate cells.
Transplantation, 28(5), 415-420 (1979-11-01)
Journal of the American Chemical Society, 125(25), 7592-7595 (2003-06-19)
A total synthesis of the laurencia metabolite (+)-obtusenyne has been completed. The key steps include a Sharpless kinetic resolution and an asymmetric glycolate alkylation to establish the stereogenic centers adjacent to the ether linkage and a ring-closing metathesis reaction to
Plant physiology and biochemistry : PPB, 130, 501-510 (2018-08-11)
Grapes are one of the most important fruits because of their economic and nutritional benefits, and grapevines are widely cultivated in arid and semi-arid areas. Therefore, it is critical to study the mechanism by which grapevines respond to water stress.
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