Cas 128552-93-2,N-[6-Methoxy-[1,2,4]thiadiazolo[3',2':2,3]thiazolo[5,4-b]pyridin-(2Z)-ylidene]-3-methyl-benzamide

128552-93-2

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Basic information

Product Name: N-[6-Methoxy-[1,2,4]thiadiazolo[3',2':2,3]thiazolo[5,4-b]pyridin-(2Z)-ylidene]-3-methyl-benzamide
Synonyms:
CAS NO:128552-93-2
Molecular Formula:
Molecular Weight: 356.429
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: N-[6-Methoxy-[1,2,4]thiadiazolo[3',2':2,3]thiazolo[5,4-b]pyridin-(2Z)-ylidene]-3-methyl-benzamide(CAS DataBase Reference)
NIST Chemistry Reference: N-[6-Methoxy-[1,2,4]thiadiazolo[3',2':2,3]thiazolo[5,4-b]pyridin-(2Z)-ylidene]-3-methyl-benzamide(128552-93-2)
EPA Substance Registry System: N-[6-Methoxy-[1,2,4]thiadiazolo[3',2':2,3]thiazolo[5,4-b]pyridin-(2Z)-ylidene]-3-methyl-benzamide(128552-93-2)

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: 128552-93-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 128552-93-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,5,5 and 2 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 128552-93:
(8*1)+(7*2)+(6*8)+(5*5)+(4*5)+(3*2)+(2*9)+(1*3)=142
142 % 10 = 2
So 128552-93-2 is a valid CAS Registry Number.

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128552-93-2Downstream Products

128552-93-2Relevant academic research and scientific papers

Synthesis of N-(2H-thiadiazolothiazolopyridin-2-ylidene)aroylamines

Sambaiah, T.,Reddy, K.Kondal

, p. 355 - 364 (2007/10/02)

The reaction of 2-aminothiazolo pyridines (1) with aroyl isothiocyanates in acetone gave N-aroyl-N'-(thiazolo pyridin-2-yl)thioureas (2).Cyclisation of 2 in the presence of PCl5 in POCl3, as well as by oxidising agents like Br2 in CHCl3, Br2 in AcOH and lead tetraacetate yielded N-(2H- thiadiazolo thiazolo pyridin-2-ylidene)aroylamines (4).

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