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关于此项目
经验公式(希尔记法):
C7H12O3
化学文摘社编号:
分子量:
144.17
UNSPSC Code:
12352005
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
5246881
Assay:
96%
Form:
liquid
Quality Level
assay
96%
form
liquid
optical activity
[α]25/D −31°, neat
refractive index
n20/D 1.428 (lit.)
bp
197 °C (lit.)
density
1.032 g/mL at 20 °C (lit.)
SMILES string
CCCC(=O)OC[C@H]1CO1
InChI
1S/C7H12O3/c1-2-3-7(8)10-5-6-4-9-6/h6H,2-5H2,1H3/t6-/m1/s1
InChI key
YLNSNVGRSIOCEU-ZCFIWIBFSA-N
Application
(R)-(-)-glycidyl butyrate undergoes hydrolysis in the presence of lipase enzyme to form (S)-(-)-glycidol. It may also be used to synthesize 1-butyroyl 2-oleoyl-3-bromo-sn-glycerol and (R)-3-(dibenzo[b,e][1,4]dioxin-7-yl)-5-(hydroxymethyl)oxazolidin-2-one.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Resp. Sens. 1 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
183.2 °F - closed cup
flash_point_c
84 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Synthesis of enantiomerically pure glycidol via a fully enantioselective lipase-catalyzed resolution.
Palomo JM, et al.
Tetrahedron Asymmetry, 16(4), 869-874 (2005)
Chiral synthesis of a triglyceride: example of 1-butyroyl 2-oleoyl 3-palmitoyl sn glycerol.
Villeneuve P, et al.
Chemistry and Physics of Lipids, 72(2), 135-141 (1994)
Synthesis of novel oxazolidinone antimicrobial agents.
Ebner DC, et al.
Bioorganic & Medicinal Chemistry, 16(5), 2651-2656 (2008)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 338125-5G | 04061837640094 |

