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邻氨基苯甲醛

邻氨基苯甲醛用途

有机合成中间体。

邻氨基苯甲醛名称

[ CAS 号 ]:
529-23-7

[ 中文名 ]:
2-氨基苯甲醛

[ 英文名 ]:
Formylaniline

[中文别名 ]:

邻氨基苯甲醛

[英文别名 ]:

Benzaldehyde, 2-amino-
2-amino-benzaldehyd
Formylaniline
2-Aminobenzaldeyhde
anthranylaldehyde
ANTHRANILALDEHYDE
MFCD00007709
o-Aminobenzaldehyde
ORTHO-AMINOBENZALDEHYDE
2-Aminobenzaldehyde

邻氨基苯甲醛物理化学性质

[ 密度 ]:
1.2±0.1 g/cm3

[ 沸点 ]:
258.7±23.0 °C at 760 mmHg

[ 熔点 ]:
38°C

[ 分子式 ]:
C₇H₇NO

[ 分子量 ]:
121.137

[ 闪点 ]:
110.2±22.6 °C

[ 精确质量 ]:
121.052765

[ PSA ]:
43.09000

[ LogP ]:
1.31

[ 外观性状 ]:
淡黄色结晶粉末

[ 蒸汽压 ]:
0.0±0.5 mmHg at 25°C

[ 折射率 ]:
1.640

[ 储存条件 ]:
−20°C

[ 稳定性 ]:
Unstable: reported to polymerize rapidly at room temperature. Incompatible with strong oxidizing agents, strong bases. Store at -20 C.

邻氨基苯甲醛MSDS

邻氨基苯甲醛安全信息

[ 符号 ]:

GHS07

[ 信号词 ]:
Warning

[ 危害声明 ]:
H315-H319-H335

[ 警示性声明 ]:
P261-P305 + P351 + P338

[ 个人防护装备 ]:
dust mask type N95 (US);Eyeshields;Gloves

[ 危害码 (欧洲) ]:
Xi:Irritant;

[ 风险声明 (欧洲) ]:
R36/37/38

[ 安全声明 (欧洲) ]:
S26-S37/39

[ 危险品运输编码 ]:
NONH for all modes of transport

[ WGK德国 ]:
3

[ 海关编码 ]:
2922399090

邻氨基苯甲醛合成路线

邻氨基苯甲醛上下游产品

邻氨基苯甲醛上游产品

邻氨基苯甲醛下游产品

邻氨基苯甲醛制备

邻硝基苯甲醛用硫酸亚铁及氨还原而得；将七水合硫酸亚铁、浓盐酸、水和邻硝基苯甲醛加入反应器中搅拌加热，当混合物温度达90℃时一次加入浓氨水，再分三批加入氨水，加料完毕，将混合物水蒸气蒸馏，馏出液用氯化钠饱和，冷却，过滤得成品。

邻氨基苯甲醛海关

[ 海关编码 ]: 2922399090

[ 中文概述 ]:
2922399090 其他氨基醛、氨基酮及其盐（包括氨基醌及其盐，但含有一种以上含氧基的除外）. 增值税率:17.0% 退税率:9.0% 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 ]:
2922399090 other amino-aldehydes, amino-ketones and amino-quinones, other than those containing more than one kind of oxygen function; salts thereof VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

邻氨基苯甲醛文献

Chondrogenesis of human bone marrow mesenchymal stromal cells in highly porous alginate-foams supplemented with chondroitin sulfate.

Mater. Sci. Eng. C. Mater. Biol. Appl. 50 , 160-72, (2015)

To overcome the limited intrinsic cartilage repair, autologous chondrocyte or bone-marrow-derived mesenchymal stromal cell (BM-MSC) was implanted into cartilage defects. For this purpose suitable bioc...

B-ring-aryl substituted luotonin A analogues with a new binding mode to the topoisomerase 1-DNA complex show enhanced cytotoxic activity.

PLoS ONE 9(5) , e95998, (2014)

Topoisomerase 1 inhibition is an important strategy in targeted cancer chemotherapy. The drugs currently in use acting on this enzyme belong to the family of the camptothecins, and suffer severe limit...

The consequences of the isotope effect on proline dehydrogenation rates estimated by the tritium loss method.

Anal. Biochem. 203(2) , 191-200, (1992)

Loss of tritium from a substrate is often used to estimate the rate of dehydrogenation. However, loss of 3H may be much slower than loss of H because of the tritium isotope effect. In order to assess ...

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