Cas 1332336-83-0,N-(3-fluorophenyl)-2-[2-oxo-5-(trifluoromethoxy)-1,2-dihydro-3H-indol-3-ylidene]-1-hydrazinecarbothioamide

1332336-83-0

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Basic information

Product Name: N-(3-fluorophenyl)-2-[2-oxo-5-(trifluoromethoxy)-1,2-dihydro-3H-indol-3-ylidene]-1-hydrazinecarbothioamide
Synonyms: N-(3-fluorophenyl)-2-[2-oxo-5-(trifluoromethoxy)-1,2-dihydro-3H-indol-3-ylidene]-1-hydrazinecarbothioamide
CAS NO:1332336-83-0
Molecular Formula:
Molecular Weight: 398.341
EINECS: N/A
Product Categories: N/A
Mol File: 1332336-83-0.mol
Article Data: 1

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: N-(3-fluorophenyl)-2-[2-oxo-5-(trifluoromethoxy)-1,2-dihydro-3H-indol-3-ylidene]-1-hydrazinecarbothioamide(CAS DataBase Reference)
NIST Chemistry Reference: N-(3-fluorophenyl)-2-[2-oxo-5-(trifluoromethoxy)-1,2-dihydro-3H-indol-3-ylidene]-1-hydrazinecarbothioamide(1332336-83-0)
EPA Substance Registry System: N-(3-fluorophenyl)-2-[2-oxo-5-(trifluoromethoxy)-1,2-dihydro-3H-indol-3-ylidene]-1-hydrazinecarbothioamide(1332336-83-0)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1332336-83-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1332336-83-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,2,3,3 and 6 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1332336-83:
(9*1)+(8*3)+(7*3)+(6*2)+(5*3)+(4*3)+(3*6)+(2*8)+(1*3)=130
130 % 10 = 0
So 1332336-83-0 is a valid CAS Registry Number.

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1332336-83-0Relevant articles and documents

Synthesis and toxicity evaluation of some N4-aryl substituted 5-trifluoromethoxyisatin-3-thiosemicarbazones

Pervez, Humayun,Saira, Naveeda,Iqbal, Mohammad Saeed,Yaqub, Muhammad,Khan, Khalid Mohammed

experimental part, p. 6408 - 6421 (2011/10/12)

A series of twenty one N4-aryl substituted 5-trifluoromethoxyisatin-3- thiosemicarbazones 3a-3u was synthesized by the reaction of trifluoromethoxyisatin 1 with different arylthiosemicarbazides 2 in aqueous ethanol (50%), containing a few drops of acetic

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