Cas 144835-94-9,(3aR,6aS)-3-(2,4-Dichloro-phenyl)-5-(3,5-dichloro-phenyl)-3a,6a-dihydro-pyrrolo[3,4-d]isoxazole-4,6-dione

144835-94-9

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Basic information

Product Name: (3aR,6aS)-3-(2,4-Dichloro-phenyl)-5-(3,5-dichloro-phenyl)-3a,6a-dihydro-pyrrolo[3,4-d]isoxazole-4,6-dione
Synonyms: (3aR,6aS)-3-(2,4-Dichloro-phenyl)-5-(3,5-dichloro-phenyl)-3a,6a-dihydro-pyrrolo[3,4-d]isoxazole-4,6-dione
CAS NO:144835-94-9
Molecular Formula:
Molecular Weight: 430.074
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (3aR,6aS)-3-(2,4-Dichloro-phenyl)-5-(3,5-dichloro-phenyl)-3a,6a-dihydro-pyrrolo[3,4-d]isoxazole-4,6-dione(CAS DataBase Reference)
NIST Chemistry Reference: (3aR,6aS)-3-(2,4-Dichloro-phenyl)-5-(3,5-dichloro-phenyl)-3a,6a-dihydro-pyrrolo[3,4-d]isoxazole-4,6-dione(144835-94-9)
EPA Substance Registry System: (3aR,6aS)-3-(2,4-Dichloro-phenyl)-5-(3,5-dichloro-phenyl)-3a,6a-dihydro-pyrrolo[3,4-d]isoxazole-4,6-dione(144835-94-9)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 144835-94-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 144835-94-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,8,3 and 5 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 144835-94:
(8*1)+(7*4)+(6*4)+(5*8)+(4*3)+(3*5)+(2*9)+(1*4)=149
149 % 10 = 9
So 144835-94-9 is a valid CAS Registry Number.

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144835-94-9Relevant academic research and scientific papers

SYNTHESIS AND FUNGICIDAL ACTIVITY OF ISOXAZOLINES FUSED TO 3,5-DICHLOROMALEIMIDE

Konopikova, Marta,Fisera, Lubor,Pronayova, Nad'a

, p. 1521 - 1536 (1992)

3-Phenyl-5-(3,5-dichlorophenyl)-3a,4,6,6a-tetrahydropyrroloisoxazoles (III, R = H) and 3-phenyl-5-(3,5-dichlorophenyl)-6a-methyl-3a,4,6,6a-tetrahydropyrroloisoxazoles (IV, R = CH3) were prepared by 1,3-dipolar cycloaddition of substituted be

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