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2,4-二甲氧基苄胺

2,4-二甲氧基苄胺名称

[ CAS 号 ]:
20781-20-8

[ 中文名 ]:
2,4-二甲氧基苯甲胺

[ 英文名 ]:
2,4-Dimethoxybenzylamine

[中文别名 ]:

2,4-二甲氧基苄胺

[英文别名 ]:

2,4-BIPYRIDINE-6-CARBOXYLIC ACID
Benzenemethanamine, 2,5-dimethoxy-
(2,4-Dimethoxyphenyl)methanamine
2,4-dimethoxy-benzylamine
Benzenemethanamine, 2,4-dimethoxy-
1-(2,5-Dimethoxyphenyl)methanamine
1-(2,4-Dimethoxyphenyl)methanamine
MFCD00052811
2,4-dimethoxybenzylamine
2,4-DIMETHOXYBENZYL AMINE

2,4-二甲氧基苄胺物理化学性质

[ 密度 ]:
1.1±0.1 g/cm3

[ 沸点 ]:
272.4±25.0 °C at 760 mmHg

[ 分子式 ]:
C₉H₁₃NO₂

[ 分子量 ]:
167.205

[ 闪点 ]:
128.4±30.4 °C

[ 精确质量 ]:
167.094635

[ PSA ]:
44.48000

[ LogP ]:
0.97

[ 外观性状 ]:
无色至淡的黄色液体至粘性液体

[ 蒸汽压 ]:
0.0±0.6 mmHg at 25°C

[ 折射率 ]:
1.523

[ 储存条件 ]:
室温

2,4-二甲氧基苄胺MSDS

2,4-二甲氧基苄胺安全信息

[ 符号 ]:

GHS05

[ 信号词 ]:
Danger

[ 危害声明 ]:
H314

[ 警示性声明 ]:
P280-P305 + P351 + P338-P310

[ 个人防护装备 ]:
Faceshields;full-face respirator (US);Gloves;Goggles;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ 危害码 (欧洲) ]:
C:Corrosive;

[ 风险声明 (欧洲) ]:
R34

[ 安全声明 (欧洲) ]:
S26-S27-S36/37/39-S45

[ 危险品运输编码 ]:
UN 2735 8/PG 3

[ WGK德国 ]:
3

[ RTECS号 ]:
DP4430000

[ 包装等级 ]:
III

[ 危险类别 ]:
8

[ 海关编码 ]:
2922299090

2,4-二甲氧基苄胺合成路线

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2,4-二甲氧基苄胺海关

[ 海关编码 ]: 2922299090

[ 中文概述 ]:
2922299090. 其他氨基(萘酚、酚)及醚、酯〔包括它们的盐, 但含有一种以上含氧基的除外〕. 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 最惠国关税:6.5%. 普通关税:30.0%

[ 申报要素 ]: 品名, 成分含量, 用途, 乙醇胺及其盐应报明色度, 乙醇胺及其盐应报明包装

[ Summary ]:
2922299090. other amino-naphthols and other amino-phenols, other than those containing more than one kind of oxygen function, their ethers and esters; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

2,4-二甲氧基苄胺文献

Total synthesis of (-)-muraymycin D2 and its epimer.

J. Org. Chem. 75(5) , 1366-77, (2010)

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 pre...

Application of the Ugi reaction for the one-pot synthesis of uracil polyoxin C analogues.

J. Org. Chem. 74(13) , 4870-3, (2009)

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'-isopropylidin...

Synthesis of N-hydroxythiourea.

J. Med. Chem. 19(2) , 336-7, (1976)

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 ...

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