258040
3,4-二甲氧基苯甲酰氯
98%
别名:
藜芦酰氯
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关于此项目
线性分子式:
(CH3O)2C6H3COCl
化学文摘社编号:
分子量:
200.62
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
222-568-0
Beilstein/REAXYS Number:
783596
MDL number:
产品名称
3,4-二甲氧基苯甲酰氯, 98%
Quality Level
InChI key
VIOBGCWEHLRBEP-UHFFFAOYSA-N
InChI
1S/C9H9ClO3/c1-12-7-4-3-6(9(10)11)5-8(7)13-2/h3-5H,1-2H3
SMILES string
COc1ccc(cc1OC)C(Cl)=O
assay
98%
form
solid
mp
70-73 °C (lit.)
functional group
acyl chloride
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Application
3,4-Dimethoxybenzoyl chloride has been used in synthesis of:
- (+)-5-(3,4-dimethoxyphenyl)-4-[[N-[(4S)-2-oxo-4-(phenylmethyl)-2-oxazolidinyl]]carbonyl] oxazole and its enantiomer
- N-(2,5-dibromophenyl)-3,4-dimethoxybenzamide
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Jian S. Tang et al.
The Journal of organic chemistry, 61(25), 8750-8754 (1996-12-13)
Both (4S-(+)-3-(isocyanoacetyl)-4-(phenylmethyl)-2-oxazolidinone (R)-1 and its enantiomer (S)-1 have been synthesized as potentially useful synthons in asymmetric synthesis. Optically active (+)-5-(3,4-dimethoxyphenyl)-4-[[N-[(4S)-2-oxo-4-(phenylmethyl)-2-oxazolidinyl]]carbonyl] oxazole (S)-2 and its enantiomer (R)-2 obtained by treating 3,4-dimethoxybenzoyl chloride with (S)-1 and (R)-1, respectively, in the presence of
Catriona G Mortimer et al.
Journal of medicinal chemistry, 49(1), 179-185 (2006-01-06)
A series of new 2-phenylbenzothiazoles has been synthesized on the basis of the discovery of the potent and selective in vitro antitumor properties of 2-(3,4-dimethoxyphenyl)-5-fluorobenzothiazole (8n; GW 610, NSC 721648). Synthesis of analogues substituted in the benzothiazole ring was achieved
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