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1H-Isoindole-1,3(2H)-dione,5,6-dichloro-

Names

[ CAS No. ]:
15997-89-4

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

[Synonym ]:
4,5-Dichlorophthalimide
3,4-dichlorophthalimide
4,5-dichlorophtalimide
5,6-dichloro-isoindole-1,3-dione
MFCD00015886
5,6-dichloroisoindoline-1,3-dione

Chemical & Physical Properties

[ Density]:
1.643g/cm3

[ Melting Point ]:
217-219ºC(lit.)

[ Molecular Formula ]:
C8H3Cl2NO2

[ Molecular Weight ]:
216.02100

[ Exact Mass ]:
214.95400

[ PSA ]:
46.17000

[ LogP ]:
2.20580

[ Index of Refraction ]:
1.637

[ Storage condition ]:
2-8℃

MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
26-36

[ RIDADR ]:
NONH for all modes of transport

[ HS Code ]:
2925190090

Synthetic Route

Precursor & DownStream

Customs

[ HS Code ]: 2925190090

[ 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%

Articles

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)


More Articles


Related Compounds

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