D167800
2,3-二甲基马来酸酐
98%
别名:
二甲基马来酸酐
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关于此项目
经验公式（希尔记法）:
C6H6O3
化学文摘社编号:
分子量:
126.11
UNSPSC Code:
12162002
NACRES:
NA.23
PubChem Substance ID:
EC Number:
212-165-8
Beilstein/REAXYS Number:
112044
MDL number:
产品名称
2,3-二甲基马来酸酐, 98%
InChI key
MFGALGYVFGDXIX-UHFFFAOYSA-N
InChI
1S/C6H6O3/c1-3-4(2)6(8)9-5(3)7/h1-2H3
SMILES string
CC1=C(C)C(=O)OC1=O
assay
98%
form
flakes
bp
223 °C (lit.)
mp
93-96 °C (lit.)
Application
用于合成马来酰亚胺类化合物以及作为超氧化物歧化酶的氨基保护剂。
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Kabrambam D Singh et al.
Scientific reports, 7(1), 12483-12483 (2017-10-04)
Evolution of resistance among insects to action of pesticides has led to the discovery of several insecticides (neonicotinoids and organophosphates) with new targets in insect nervous system. Present study evaluates the mode of inhibition of acetylchlonesterase (AChE), biochemical efficacy, and
S Tsunoda et al.
The Journal of pharmacology and experimental therapeutics, 290(1), 368-372 (1999-06-25)
We attempted to develop a novel method for the chemical modification of cytokines with synthetic polymers to increase in vivo therapeutic efficacy. A pH-reversible amino-protective reagent, dimethylmaleic anhydride (DMMAn), was used for polymer conjugation of tumor necrosis factor-alpha (TNF-alpha) with
Se Rim Yoon et al.
Journal of biomedical materials research. Part A, 100(8), 2027-2033 (2012-05-15)
A charge-converting and pH-dependent nanocarrier was achieved by conjugating 2,3-dimethylmaleic anhydride (DMMA) to the amino group of an octadecyl grafted poly (2-hydroxyethyl aspartamide) (PHEA-g-C(18)-NH(2)) backbone, thereby forming a spherical micelle. PHEA, a poly(amino acid)s derivative, was derived from poly(succinimide), which
C Vard et al.
The Journal of biological chemistry, 272(32), 20259-20262 (1997-08-08)
The acidic ribosomal proteins P1-P2 from rat liver were overproduced for the first time by expression of their cDNA in Escherichia coli. They were tested for their ability to reactivate inactive P1-P2-deficient core particles derived from 60 S ribosomal subunits
J. Controlled Release, 28, 203-203 (1994)
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