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4-甲氧苄基异氰酸酯

4-甲氧苄基异氰酸酯名称

[ CAS 号 ]:
56651-60-6

[ 中文名 ]:
4-甲氧苄基异氰酸酯

[ 英文名 ]:
p-Methoxybenzyl isocyanate

[中文别名 ]:

[英文别名 ]:

MFCD00673064
1-(Isocyanatomethyl)-4-methoxybenzene
p-Methoxybenzyl isocyanate
Benzene, 1-(isocyanatomethyl)-4-methoxy-
4-(Isocyanatomethyl)phenyl methyl ether

4-甲氧苄基异氰酸酯物理化学性质

[ 密度 ]:
1.0±0.1 g/cm3

[ 沸点 ]:
249.9±23.0 °C at 760 mmHg

[ 分子式 ]:
C₉H₉NO₂

[ 分子量 ]:
163.173

[ 闪点 ]:
112.6±17.1 °C

[ 精确质量 ]:
163.063324

[ PSA ]:
38.66000

[ LogP ]:
2.52

[ 外观性状 ]:
透明无色至黄色液体

[ 蒸汽压 ]:
0.0±0.5 mmHg at 25°C

[ 折射率 ]:
1.507

[ 储存条件 ]:
2-8°C

4-甲氧苄基异氰酸酯安全信息

[ 符号 ]:

GHS07, GHS08

[ 信号词 ]:
Danger

[ 危害声明 ]:
H302-H312-H315-H319-H332-H334-H335

[ 警示性声明 ]:
P261-P280-P305 + P351 + P338-P342 + P311

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

[ 危害码 (欧洲) ]:
Xn:Harmful;

[ 风险声明 (欧洲) ]:
R20/21/22;R36/37/38;R42

[ 安全声明 (欧洲) ]:
S26-S36/37/39

[ 危险品运输编码 ]:
UN 2206PSN1B 6.1 / PGIII

[ WGK德国 ]:
3

[ 海关编码 ]:
2929109000

4-甲氧苄基异氰酸酯合成路线

详细合成路线

4-甲氧苄基异氰酸酯上下游产品

4-甲氧苄基异氰酸酯上游产品

4-甲氧苄基异氰酸酯下游产品

4-甲氧苄基异氰酸酯海关

[ 海关编码 ]: 2929109000

[ 中文概述 ]:
2929109000. 其他异氰酸酯. 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

[ Summary ]:
2929109000. other isocyanates. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

4-甲氧苄基异氰酸酯文献

Discovery of nitroaryl urea derivatives with antiproliferative properties.

J. Enzyme Inhib. Med. Chem. , 1-11, (2015)

A series of urea derivatives bearing nitroaryl moiety has been synthesized and assayed for their potential antiproliferative activities. Some of the tested compounds displayed activity in RK33 larynge...

The first synthesis of a novel 5:7:5-fused diimidazodiazepine ring system and some of its chemical properties.

Org. Lett. 10(20) , 4681-4, (2008)

The first synthesis of a novel 5:7:5-fused heterocyclic ring system, a diimidazodiazepine, is reported. The propensity of the ring system to undergo facile, acid-catalyzed nucleophilic addition reacti...

Total synthesis of (+)-batzelladine A and (-)-batzelladine D via [4 + 2]-annulation of vinyl carbodiimides with N-alkyl imines.

J. Am. Chem. Soc. 128 , 13255, (2006)

A diastereoselective [4 + 2]-annulation of vinyl carbodiimides with chiral N-alkyl imines has been developed to access the stereochemically rich polycyclic guanidine cores of the batzelladine alkaloid...

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