D130400
2,4-二甲氧基苯甲醛
98%
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线性分子式:
(CH3O)2C6H3CHO
化学文摘社编号:
分子量:
166.17
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-342-4
Beilstein/REAXYS Number:
607989
MDL number:
产品名称
2,4-二甲氧基苯甲醛, 98%
InChI key
LWRSYTXEQUUTKW-UHFFFAOYSA-N
InChI
1S/C9H10O3/c1-11-8-4-3-7(6-10)9(5-8)12-2/h3-6H,1-2H3
SMILES string
COc1ccc(C=O)c(OC)c1
assay
98%
form
crystals
bp
165 °C/10 mmHg (lit.)
mp
67-69 °C (lit.)
Quality Level
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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
Francesca Rosi et al.
Analytical and bioanalytical chemistry, 409(12), 3187-3197 (2017-03-08)
A new analytical approach, based on micro-transflection measurements from a diamond-coated metal sampling stick, is presented for the analysis of painting varnishes. Minimally invasive sampling is performed from the varnished surface using the stick, which is directly used as a
Outi Keinänen et al.
Nuclear medicine and biology, 67, 27-35 (2018-11-01)
18F-fluoroglycosylation via oxime formation is a chemoselective and mild radiolabeling method for sensitive molecules. Glycosylation can also improve the bioavailability, in vivo kinetics, and stability of the compound in blood, as well as accelerate clearance of biomolecules. A typical synthesis
Lidia Montero et al.
Journal of chromatography. A, 1428, 115-125 (2015-07-27)
In the present work, the phlorotannin composition of different Sargassum muticum samples collected at different locations along the North Atlantic coasts as well as the bioactivities related to these components were investigated. After pressurized liquid extraction, the samples collected at
J Blaakmeer et al.
International journal of peptide and protein research, 37(6), 556-564 (1991-06-01)
The synthesis of the model compound Aloc-Ala-Ala-Dma-Ala-Ala-OMe has been described as an illustration of the fact that a large group reversibly alkylating the amido group of an oligomer can disturb the regularity of a peptide backbone, oppose its aggregation and
Gustavo P B Carretero et al.
Biochimica et biophysica acta. Biomembranes, 1860(8), 1502-1516 (2018-05-12)
Antimicrobial peptides (AMPs) work as a primary defense against pathogenic microorganisms. BP100, (KKLFKKILKYL-NH2), a rationally designed short, highly cationic AMP, acts against many bacteria, displaying low toxicity to eukaryotic cells. Previously we found that its mechanism of action depends on
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