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化驗
97%
折射率
n20/D 1.432 (lit.)
bp
169 °C (lit.)
密度
0.75 g/mL at 25 °C (lit.)
SMILES 字串
C=CCCCCCCC=C
InChI
1S/C10H18/c1-3-5-7-9-10-8-6-4-2/h3-4H,1-2,5-10H2
InChI 密鑰
NLDGJRWPPOSWLC-UHFFFAOYSA-N
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一般說明
1,9-Decadiene acts as comonomer and undergoes acyclic diene metathesis (ADMET) copolymerization with 1, 5-hexadiene to form random linear polybutadiene –polyoctenamer copolymers. It undergoes ADMET copolymerization with divinyltetraethoxydisiloxane to yield siloxylene–vinylene–alkenylene copolymer.
應用
1,9-Decadiene was used in synthesis and characterization of new telechelic polyoctenamers prepared by ADMET polymerization using Grubbs catalyst.
訊號詞
Warning
危險分類
Aquatic Acute 1 - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
3 - Flammable liquids
水污染物質分類（WGK）
WGK 3
閃點（°F）
105.8 °F - closed cup
閃點（°C）
41 °C - closed cup
個人防護裝備
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
其他客户在看
ADMET copolymerization of divinyltetraethoxydisiloxane with 1, 9-decadiene catalyzed by Grubbs' catalyst.
Malecka E, et al.
J. Mol. Catal. A: Chem., 190(1), 27-31 (2002)
Acyclic diene metathesis copolymerization of 1, 5-hexadiene and 1, 9-decadiene.
Wagener KB, et al.
Macromolecules, 23(24), 5155-5157 (1990)
Brent L Lee et al.
The Journal of chemical physics, 144(24), 245103-245103 (2016-07-03)
The time-resolved parallel artificial membrane permeability assay with fluorescence detection and comprehensive computer simulations are used to study the passive permeation of three aromatic dipeptides-N-acetyl-phenylalanineamide (NAFA), N-acetyltyrosineamide (NAYA), and N-acetyl-tryptophanamide (NATA) through a 1,2-dioleoyl-sn-glycero-3-phospocholine (DOPC) lipid bilayer. Measured permeation times
Synthesis of ABA triblock copolymers via acyclic diene metathesis polymerization and living polymerization of a-amino acid-N-carboxyanhydrides.
Brzezinska KR and Deming TJ.
Macromolecules, 34(13), 4348-4354 (2001)
Shuzhe Wang et al.
Journal of medicinal chemistry, 64(17), 12761-12773 (2021-08-19)
Cyclic peptides have received increasing attention over the recent years as potential therapeutics for "undruggable" targets. One major obstacle is, however, their often relatively poor bioavailability. Here, we investigate the structure-permeability relationship of 24 cyclic decapeptides that share the same
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