Cas 90235-02-2,2H-Isoindole-2-carboximidothioic acid, 1,3-dihydro-N-(4-nitrobenzoyl)-, 4-methylphenyl ester

90235-02-2

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Basic information

Product Name: 2H-Isoindole-2-carboximidothioic acid, 1,3-dihydro-N-(4-nitrobenzoyl)-, 4-methylphenyl ester
Synonyms:
CAS NO:90235-02-2
Molecular Formula: C23H19N3O3S
Molecular Weight: 417.488
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: 2H-Isoindole-2-carboximidothioic acid, 1,3-dihydro-N-(4-nitrobenzoyl)-, 4-methylphenyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2H-Isoindole-2-carboximidothioic acid, 1,3-dihydro-N-(4-nitrobenzoyl)-, 4-methylphenyl ester(90235-02-2)
EPA Substance Registry System: 2H-Isoindole-2-carboximidothioic acid, 1,3-dihydro-N-(4-nitrobenzoyl)-, 4-methylphenyl ester(90235-02-2)

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: 90235-02-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 90235-02-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,2,3 and 5 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 90235-02:
(7*9)+(6*0)+(5*2)+(4*3)+(3*5)+(2*0)+(1*2)=102
102 % 10 = 2
So 90235-02-2 is a valid CAS Registry Number.

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90235-02-2Downstream Products

90235-02-2Relevant academic research and scientific papers

Synthesis of New Carboximidoyl Chlorides and Their Reaction with Nucleophiles

Ried, Walter,Kuembel, Brigitte,Tauer, Marie-Luise

, p. 564 - 575 (2007/10/02)

One-step reactions of N,N-dialkylcyanamides 1a-c and dicarbonitriles 1d, e with organic acyl chlorides and with 2-chloro-1,1-dicyanoethylenes easily lead to the N-acyl-substituted carboximidoyl chlorides 2a-k and biscarboximidoyl chlorides 2l-v, respectively.The substituents in the α-position of the chlorocarbonyl group have a strong influence on the stability of the reaction products.The carboximidoyl chlorides 2a, f, o, and u react with O-nucleophiles (H2O, alcohols, phenols), S-nucleophiles (dithiocarbamates, thiophenols), and N-nucleophiles (NH3, aliphatic and aromatic amines) to give a variety of products.

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