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About This Item
经验公式（希尔记法）:
C7H12O3
CAS号:
分子量:
144.17
Beilstein:
5246881
MDL號碼:
分類程式碼代碼:
12352005
PubChem物質ID:
NACRES:
NA.22
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品質等級
化驗
96%
形狀
liquid
光學活性
[α]25/D −31°, neat
折射率
n20/D 1.428 (lit.)
bp
197 °C (lit.)
密度
1.032 g/mL at 20 °C (lit.)
SMILES 字串
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 密鑰
YLNSNVGRSIOCEU-ZCFIWIBFSA-N
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應用
(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.
訊號詞
Danger
危險分類
Acute Tox. 4 Oral - Eye Irrit. 2 - Resp. Sens. 1 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
10 - Combustible liquids
水污染物質分類（WGK）
WGK 3
閃點（°F）
183.2 °F - closed cup
閃點（°C）
84 °C - closed cup
個人防護裝備
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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)
Synthesis of enantiomerically pure glycidol via a fully enantioselective lipase-catalyzed resolution.
Palomo JM, et al.
Tetrahedron Asymmetry, 16(4), 869-874 (2005)
Arnaldo Glogauer et al.
Microbial cell factories, 10, 54-54 (2011-07-19)
Metagenomics, the application of molecular genomics to consortia of non-cultivated microbes, has the potential to have a substantial impact on the search for novel industrial enzymes such as esterases (carboxyl ester hydrolases, EC 3.1.1.1) and lipases (triacylglycerol lipases, EC 3.1.1.3).
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