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经验公式(希尔记法):
C15H20O4
化学文摘社编号:
分子量:
264.32
UNSPSC Code:
12352200
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
5481541
grade
derivatization grade ((chiral))
Quality Level
assay
≥99.0% (sum of enantiomers, HPLC), ≥99.0%
form
powder
optical activity
[α]20/D +69±2°, c = 1% in ethanol
optical purity
enantiomeric ratio: ≥99.5:0.5 (HPLC)
quality
LiChropur™
mp
149-155 °C
SMILES string
COc1c(C)c(C)c2O[C@](C)(CCc2c1C)C(O)=O
InChI
1S/C15H20O4/c1-8-9(2)13-11(10(3)12(8)18-5)6-7-15(4,19-13)14(16)17/h6-7H2,1-5H3,(H,16,17)/t15-/m1/s1
InChI key
MNBMVDGIDVXTOF-OAHLLOKOSA-N
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
此项目有
Peter V Cornish et al.
Molecular cell, 30(5), 578-588 (2008-06-10)
During the elongation cycle, tRNA and mRNA undergo coupled translocation through the ribosome catalyzed by elongation factor G (EF-G). Cryo-EM reconstructions of certain EF-G-containing complexes led to the proposal that the mechanism of translocation involves rotational movement between the two