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4,5-二氯酞酰亚胺

4,5-二氯酞酰亚胺名称

[ CAS 号 ]:
15997-89-4

[ 中文名 ]:
4,5-二氯酞酰亚胺

[ 英文名 ]:
1H-Isoindole-1,3(2H)-dione,5,6-dichloro-

[中文别名 ]:

4,5-二氯邻苯二甲酰亚胺

[英文别名 ]:

4,5-Dichlorophthalimide
3,4-dichlorophthalimide
4,5-dichlorophtalimide
5,6-dichloro-isoindole-1,3-dione
MFCD00015886
5,6-dichloroisoindoline-1,3-dione

4,5-二氯酞酰亚胺物理化学性质

[ 密度 ]:
1.643g/cm3

[ 熔点 ]:
217-219ºC(lit.)

[ 分子式 ]:
C₈H₃Cl₂NO₂

[ 分子量 ]:
216.02100

[ 精确质量 ]:
214.95400

[ PSA ]:
46.17000

[ LogP ]:
2.20580

[ 折射率 ]:
1.637

[ 储存条件 ]:
2-8℃

4,5-二氯酞酰亚胺MSDS

4,5-二氯酞酰亚胺安全信息

[ 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) ]:
26-36

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

[ 海关编码 ]:
2925190090

4,5-二氯酞酰亚胺合成路线

4,5-二氯酞酰亚胺上下游产品

4,5-二氯酞酰亚胺上游产品

4,5-二氯酞酰亚胺下游产品

4,5-二氯酞酰亚胺海关

[ 海关编码 ]: 2925190090

[ 中文概述 ]:
2925190090 其他酰亚胺及其衍生物盐. 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

[ Summary ]:
2925190090 other imides and their derivatives; salts thereof VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

4,5-二氯酞酰亚胺文献

Phosphine-catalyzed allylic substitution of Morita-Baylis-Hillman acetates: synthesis of N-protected beta-aminophosphonic acid esters.

J. Org. Chem. 71(20) , 7892-7894, (2006)

A series of N-protected beta-amino phosphonic acid esters have been prepared by phosphine-catalyzed allylic substitution of 2-(diethylphosphonyl)-substituted allylic acetates employing 4,5-dichloropht...

Synthesis and antiviral activity of some 5'-N-phthaloyl-3'-azido-2',3'-dideoxythymidine analogues.

Antivir. Chem. Chemother. 14(3) , 139-144, (2003)

A variety of substituted 5'-N-phthaloyl-3'-azido-2',3'-dideoxythymidine derivatives has been evaluated for their activity against HIV-1, HIV-2 and Moloney murine sarcoma virus (MSV) in cell culture. M...

Synthesis of water soluble PEGylated (copper) phthalocyanines via Mitsunobu reaction and Cu (i)-catalysed azide-alkyne cycloaddition (CuAAC) click chemistry. Li M, et al.

Polym. Chem. 4(16) , 4405-4411, (2013)

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