38619
2,4-二甲氧基苯甲醛
purum, ≥97.0% (T)
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线性分子式:
(CH3O)2C6H3CHO
化学文摘社编号:
分子量:
166.17
EC Number:
210-342-4
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
607989
MDL number:
grade
purum
assay
≥97.0% (T)
bp
165 °C/10 mmHg (lit.)
mp
67-69 °C (lit.), 67-70 °C
SMILES string
COc1ccc(C=O)c(OC)c1
InChI
1S/C9H10O3/c1-11-8-4-3-7(6-10)9(5-8)12-2/h3-6H,1-2H3
InChI key
LWRSYTXEQUUTKW-UHFFFAOYSA-N
法规信息
新产品
此项目有
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
Ulrik Boas et al.
Journal of combinatorial chemistry, 4(3), 223-228 (2002-05-15)
The tris(alkoxy)benzyl backbone amide linker (BAL) has found widespread application in solid-phase synthesis. The key intermediate for preparation of para BAL (p-BAL) is 2,6-dimethoxy-4-hydroxybenzaldehyde; several reports on its synthesis have appeared. However, the ortho analogue of the handle (o-BAL) has
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