Cas 79560-75-1,Hydrazinecarbothioamide, 2-(1,2-dihydro-1-methyl-2-oxo-3H-indol-3-ylidene)-N-phenyl-

79560-75-1

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Basic information

Product Name: Hydrazinecarbothioamide, 2-(1,2-dihydro-1-methyl-2-oxo-3H-indol-3-ylidene)-N-phenyl-
Synonyms: 1-methyl-1H-indole-2,3-dione 3-(N-phenylthiosemicarbazone);Hydrazinecarbothioamide, 2-(1,2-dihydro-1-methyl-2-oxo-3H-indol-3-ylidene)-N-phenyl-
CAS NO:79560-75-1
Molecular Formula: C₁₆H₁₄N₄OS
Molecular Weight: 310.37
EINECS: N/A
Product Categories: N/A
Mol File: 79560-75-1.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: Hydrazinecarbothioamide, 2-(1,2-dihydro-1-methyl-2-oxo-3H-indol-3-ylidene)-N-phenyl-(CAS DataBase Reference)
NIST Chemistry Reference: Hydrazinecarbothioamide, 2-(1,2-dihydro-1-methyl-2-oxo-3H-indol-3-ylidene)-N-phenyl-(79560-75-1)
EPA Substance Registry System: Hydrazinecarbothioamide, 2-(1,2-dihydro-1-methyl-2-oxo-3H-indol-3-ylidene)-N-phenyl-(79560-75-1)

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: 79560-75-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 79560-75-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,5,6 and 0 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 79560-75:
(7*7)+(6*9)+(5*5)+(4*6)+(3*0)+(2*7)+(1*5)=171
171 % 10 = 1
So 79560-75-1 is a valid CAS Registry Number.

79560-75-1Upstream product

79560-75-1Downstream Products

79560-75-1Relevant academic research and scientific papers

Isatin-β-thiosemicarbazones as potent herpes simplex virus inhibitors

Kang, Iou-Jiun,Wang, Li-Wen,Hsu, Tsu-An,Yueh, Andrew,Lee, Chung-Chi,Lee, Yen-Chun,Lee, Ching-Yin,Chao, Yu-Sheng,Shih, Shin-Ru,Chern, Jyh-Haur

, p. 1948 - 1952 (2011/05/04)

A series of isatin-β-thiosemicarbazones have been designed and evaluated for antiviral activity against herpes simplex virus type 1 (HSV-1) and type 2 (HSV-2) in a plaque reduction assay. Their cytotoxicity was examined using human rhabdomyosarcoma cells (RD cells). Several derivatives of isatin-β-thiosemicarbazone exhibited significant and selective antiviral activity with low cytotoxicity. It was found that the thiourea group at thiosemicarbazone and the NH functionality at isatin were essential for their antiherpetic activity. The synthesis and structure-activity relationship studies are presented.

Synthesis of Spirothiadiazoline>-2-ones by Acetylation of Isatin-β-thiosemicarbazones

Somogyi, Laszlo

, p. 931 - 934 (2007/10/02)

The synthesis of spirothiadiazoline>-2-ones 2a-g by cyclization of isatin-β-thiosemicarbazones 1a-f is reported.The structure determination of 2a-g by IR, (1)H- and (13)C-NMR measurements is also described. Key words: Acetylation; isatin; 1,3,4-thiadiazolines; thiosemicarbazones, cyclization of

Syntheses of some substituted isatin-β-thiosemicarbazones and isatin-β-hydrazonothiazoline derivatives as potential antiviral and antimicrobial agents

Omar,Eshba,Salama

, p. 701 - 709 (2007/10/02)

A series of isatin-β-thioxemicarbazones and isatin-β-hydrazonothiazolines was synthesized by condensation of various isatin derivatives with N4-substituted-3-thiosemicarbazides and cyclization of the products by phenacyl bromides. The products

Reactions of 3-Arylimino-2-Indolinones with p-Substituted Phenylthiosemicarbazides

Varma, Rajendra S.,Garg, Pradeep K.

, p. 980 - 981 (2007/10/02)

3-Arylimino-2-indolinones (II) have been prepared by the condensation of isatins (I) with anilines.Reactions of II with p-substituted phenylthiosemicarbazides have resulted (in every instance) in the displacement of arylimino groups by the phenylthiosemic

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