V900554
戊二酸酐
Vetec™, reagent grade, 94%
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经验公式（希尔记法）:
C5H6O3
化学文摘社编号:
分子量:
114.10
EC Number:
203-593-6
UNSPSC Code:
12162002
PubChem Substance ID:
Beilstein/REAXYS Number:
110051
MDL number:
InChI key
VANNPISTIUFMLH-UHFFFAOYSA-N
InChI
1S/C5H6O3/c6-4-2-1-3-5(7)8-4/h1-3H2
SMILES string
O=C1CCCC(=O)O1
grade
reagent grade
product line
Vetec™
assay
94%
bp
150 °C/10 mmHg (lit.)
mp
50-55 °C (lit.)
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Legal Information
Vetec is a trademark of Merck KGaA, Darmstadt, Germany
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
H B Lazrek et al.
Nucleosides, nucleotides & nucleic acids, 26(8-9), 1103-1106 (2007-12-07)
We report the synthesis of homo and heterodimers of 3TC conjugates. All new dimers were screened for their ability to inhibit HIV-1 in MT4 cell line and were compared to AZT alone and showed marked antiviral activity.
B Ballantyne et al.
Veterinary and human toxicology, 34(6), 493-497 (1992-12-01)
Glutaric anhydride (GA), an industrial chemical, was found of moderate acute peroral lethal toxicity with LD50 values (95% confidence limits) in the rat of 1.41 (0.80-2.49) g/kg (males) and 0.54 (0.36-0.79) g/kg (females), with death being due in part to
Jaleh Varshosaz et al.
Journal of drug targeting, 19(2), 140-153 (2010-05-01)
An oral colon-targeted formulation of budesonide was developed for treatment of ulcerative colitis. Budesonide conjugates were prepared using glutarate spacer and different molecular weights (MW) of dextran and their degree of substitution (DS), solubility, and stability were examined. Drug release
T Tanaka et al.
Biological & pharmaceutical bulletin, 16(12), 1270-1275 (1993-12-01)
The tumor distribution and the disposition of serum proteins, such as albumin, fetuin, transferrin, and IgG, were investigated in mice bearing Sarcoma 180. Serum proteins labeled with fluoresceinisothiocyanate (FITC) were administered to the mice. The FITC-labeled proteins acylated with glutaric
Purushothaman Gopinath et al.
Organic letters, 14(5), 1358-1361 (2012-02-22)
We describe the desymmetrization of meso-glutaric anhydrides to chiral hemiesters using a bench-stable homodinuclear Ni(2)-(Schiff base) complex as the catalyst in good to excellent yield (up to 99%) and enantioselectivity (up to 94%). Using the opposite enantiomer of the catalyst
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