432725
2,4-二甲氧基苄胺
98%
别名:
1-（2,4-二甲氧基苯基）甲胺, 2,4-二甲基氧基苄胺, 2,4-二甲氧基苯甲胺, [(2,4-二甲氧基苯基)甲基]胺, （2,4-二甲氧基苯基）甲胺
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关于此项目
线性分子式:
(CH3O)2C6H3CH2NH2
化学文摘社编号:
分子量:
167.21
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
98%
InChI
1S/C9H13NO2/c1-11-8-4-3-7(6-10)9(5-8)12-2/h3-5H,6,10H2,1-2H3
SMILES string
COc1ccc(CN)c(OC)c1
InChI key
QOWBXWFYRXSBAS-UHFFFAOYSA-N
assay
98%
refractive index
n20/D 1.549 (lit.)
bp
140 °C/1 mmHg (lit.)
density
1.113 g/mL at 25 °C (lit.)
functional group
amine
Quality Level
General description
2,4-二甲氧基苄胺可以通过还原（NaBH4，BF3.OEt2,，THF）2,4-二甲氧基苄腈来制备。
Application
2,4-二甲氧基苄胺是一种胺亲核试剂，用于研究5-溴-2-茚-1-酮的 1,4- 反应性。它可用于以下研究：
- 作为一系列 2,4,5-三取代恶唑的简明合成中的氨当量，通过串联 Ugi/Robinson-Gabriel 反应序列。
- 全合成（-）-muraymycin（MRY）D2 及其差向异构体，抗菌核苷天然产物。
- 使用 Ugi 反应，两步法合成尿嘧啶多氧霉素 C（UPOC）甲酯的酰胺衍生物。
- N-羟基硫脲的合成。
- 合成抗 HIV-1 试剂。
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Tetrahedron Letters, 47, 8459-8459 (2006)
Tetsuya Tanino et al.
The Journal of organic chemistry, 75(5), 1366-1377 (2010-02-11)
Full details of the first total synthesis of (-)-muraymycin (MRY) D2 and its epimer, the antibacterial nucleoside natural product, are described. Key strategic elements of the approach include the preparation of the urea dipeptide moiety found in the muraymycins containing
Arthur Y Shaw et al.
Tetrahedron letters, 53(15), 1998-2000 (2013-04-06)
This Letter discloses a novel concise synthesis of a series of 2,4,5-trisubstituted oxazoles via a tandem Ugi/Robinson-Gabriel sequence. Herein, 2,4-dimethoxybenzylamine
M Sato et al.
Journal of medicinal chemistry, 19(2), 336-337 (1976-02-01)
The synthesis of the title compound (1) was accomplished by the conversion of 2,4-dimethoxybenzylamine (2) into an isothiocyanate (3) using thiocarbonyl diimidazole. Treatment of 3 with hydroxylamine and removal of the DMB group with trifluoroacetic acid gave 1. N-Hydroxythiourea (1)
Andrew Plant et al.
The Journal of organic chemistry, 74(13), 4870-4873 (2009-05-22)
A simple, two-step synthesis of amide derivatives of uracil polyoxin C (UPOC) methyl ester using the Ugi reaction is described. The four components employed in the Ugi reaction are 2',3'-isopropylidine-protected uridine-5'-aldehyde, 2,4-dimethoxybenzylamine, an isoxazolecarboxylic acid, and the convertible isonitrile N-(2-{[(tert-butyldimethylsilyl)oxy]methyl}phenyl)carbonitrile.
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