666955
4-(Trimethylsilyl)-3-butyn-2-ol
97%
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About This Item
Fórmula empírica (notación de Hill):
C7H14OSi
Número de CAS:
Peso molecular:
142.27
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
Productos recomendados
assay
97%
refractive index
n20/D 1.446
density
0.847 g/mL at 25 °C
functional group
hydroxyl
storage temp.
2-8°C
SMILES string
CC(O)C#C[Si](C)(C)C
InChI
1S/C7H14OSi/c1-7(8)5-6-9(2,3)4/h7-8H,1-4H3
InChI key
HJJSDJHRTMFJLP-UHFFFAOYSA-N
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
10 - Combustible liquids
wgk_germany
WGK 3
flash_point_f
143.0 °F - closed cup
flash_point_c
61.67 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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Bo-Bo Zhang et al.
PloS one, 7(5), e37641-e37641 (2012-06-05)
Hydrophilic ionic liquids (ILs) were employed as green solvents to construct an IL-containing co-solvent system for improving the asymmetric reduction of 4-(trimethylsilyl)-3-butyn-2-one by immobilized Candida parapsilosis cells. Among 14 hydrophilic ILs examined, 1-(2'-hydroxyl)ethyl-3-methylimidazolium nitrate (C(2)OHMIM·NO(3)) was considered as the most
Wen-Yong Lou et al.
BMC biotechnology, 9, 90-90 (2009-10-24)
Whole cells are usually employed for biocatalytic reduction reactions to ensure efficient coenzyme regeneration and to avoid problems with enzyme purification and stability. The efficiency of whole cell-catalyzed bioreduction is frequently restricted by pronounced toxicity of substrate and/or product to
Xiao-Hong Chen et al.
BMC biotechnology, 11, 110-110 (2011-11-22)
Chiral alcohols are widely used in the synthesis of chiral pharmaceuticals, flavors and functional materials and appropriate whole-cell biocatalysts offer a highly enantioselective, minimally polluting route to these valuable compounds. The recently isolated strain Acetobacter sp. CCTCC M209061 showed exclusive
Xiao-Hong Chen et al.
PloS one, 9(4), e94543-e94543 (2014-04-18)
A novel carbonyl reductase (AcCR) catalyzing the asymmetric reduction of ketones to enantiopure alcohols with anti-Prelog stereoselectivity was found in Acetobacter sp. CCTCC M209061 and enriched 27.5-fold with an overall yield of 0.4% by purification. The enzyme showed a homotetrameric
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