Cas 1293364-32-5,N-(5-chloro-2-methylphenyl)-2-[2-oxo-5-(trifluoromethoxy)-1,2-dihydro-3H-indol-3-ylidene]-1-hydrazinecarbothioamide

1293364-32-5

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Basic information

Product Name: N-(5-chloro-2-methylphenyl)-2-[2-oxo-5-(trifluoromethoxy)-1,2-dihydro-3H-indol-3-ylidene]-1-hydrazinecarbothioamide
Synonyms:
CAS NO:1293364-32-5
Molecular Formula:
Molecular Weight: 428.822
EINECS: N/A
Product Categories: N/A
Mol File: 1293364-32-5.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-(5-chloro-2-methylphenyl)-2-[2-oxo-5-(trifluoromethoxy)-1,2-dihydro-3H-indol-3-ylidene]-1-hydrazinecarbothioamide(CAS DataBase Reference)
NIST Chemistry Reference: N-(5-chloro-2-methylphenyl)-2-[2-oxo-5-(trifluoromethoxy)-1,2-dihydro-3H-indol-3-ylidene]-1-hydrazinecarbothioamide(1293364-32-5)
EPA Substance Registry System: N-(5-chloro-2-methylphenyl)-2-[2-oxo-5-(trifluoromethoxy)-1,2-dihydro-3H-indol-3-ylidene]-1-hydrazinecarbothioamide(1293364-32-5)

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: 1293364-32-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1293364-32-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,9,3,3,6 and 4 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1293364-32:
(9*1)+(8*2)+(7*9)+(6*3)+(5*3)+(4*6)+(3*4)+(2*3)+(1*2)=165
165 % 10 = 5
So 1293364-32-5 is a valid CAS Registry Number.

1293364-32-5Upstream product

169037-23-4 5-trifluoromethoxy-1H-indole-2,3-dione

1293364-32-5Downstream Products

1293364-32-5Relevant 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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