推薦產品
品質等級
化驗
98%
形狀
solid
光學活性
[α]20/D +35.1°, c = 20 in ethanol
bp
219 °C (lit.)
mp
51-53 °C (lit.)
SMILES 字串
C[C@@H]1[C@@H](O)CC2CC1C2(C)C
InChI
1S/C10H18O/c1-6-8-4-7(5-9(6)11)10(8,2)3/h6-9,11H,4-5H2,1-3H3/t6-,7+,8-,9-/m0/s1
InChI 密鑰
REPVLJRCJUVQFA-KZVJFYERSA-N
一般說明
(1S,2S,3S,5R)-(+)-Isopinocampheol is a chiral terpenol.[1]
應用
(1S,2S,3S,5R)-(+)-Isopinocampheol may be used in the preparation of
- thermotropic chiral nematic side-chain copolymers[2]
- ortho-(diphenylphosphino)phenylphosphonous acid di[(1S,2S,3S,5R)-2,6,6-trimethyl-bicyclo[3.1.1]-hept-3-yl]ester, a phosphino-phosphonite ligand[3]
- O,O´bis[(1S,2S,3S,5R)2,6,6-trimethylbicyclo[3.1.1]hept-3-yl] dithiophosphoric acid, a bioactive compound with antifungal effect[4]
儲存類別代碼
11 - Combustible Solids
水污染物質分類(WGK)
WGK 3
閃點(°F)
200.1 °F - closed cup
閃點(°C)
93.4 °C - closed cup
個人防護裝備
Eyeshields, Gloves, type N95 (US)
New thermotropic chiral nematic copolymers using (1S, 2S, 3S, 5R)-(+)-and (1R, 2R, 3R, 5S)-([minus])-isopinocampheol as building blocks.
Chen SH and Tsai ML.
Macromolecules, 23(24) (1990)
Synthesis of enantiopure C 1 symmetric diphosphines and phosphino-phosphonites with ortho-phenylene backbones.
Kottsieper KW, et al.
Tetrahedron Asymmetry, 12(8), 1159-1169 (2001)
Chiral phosphorus dithio acids derived from (1S, 2S, 3S, 5R)-(+)-isopinocampheol. Synthesis and fungicidal activity.
Nizamov IS, et al.
Russian Chemical Bulletin, 61(12), 2370-2371 (2012)
Terpene Analogues of Dithiophospate Pesticides.
Cherkasov RA, et al.
Phosph. Sulfur Relat. Elem., 186(4), 1003-1004 (2011)
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