Cas 1287701-48-7,(Z)-2-(4-chlorobenzylidene)-5-(3,4-dimethoxyphenyl)-8,8-dimethyl-8,9-dihydro-2H-thiazolo[2,3-b]quinazoline-3,6(5H,7H)-dione

1287701-48-7

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Basic information

Product Name: (Z)-2-(4-chlorobenzylidene)-5-(3,4-dimethoxyphenyl)-8,8-dimethyl-8,9-dihydro-2H-thiazolo[2,3-b]quinazoline-3,6(5H,7H)-dione
Synonyms:
CAS NO:1287701-48-7
Molecular Formula:
Molecular Weight: 509.025
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: (Z)-2-(4-chlorobenzylidene)-5-(3,4-dimethoxyphenyl)-8,8-dimethyl-8,9-dihydro-2H-thiazolo[2,3-b]quinazoline-3,6(5H,7H)-dione(CAS DataBase Reference)
NIST Chemistry Reference: (Z)-2-(4-chlorobenzylidene)-5-(3,4-dimethoxyphenyl)-8,8-dimethyl-8,9-dihydro-2H-thiazolo[2,3-b]quinazoline-3,6(5H,7H)-dione(1287701-48-7)
EPA Substance Registry System: (Z)-2-(4-chlorobenzylidene)-5-(3,4-dimethoxyphenyl)-8,8-dimethyl-8,9-dihydro-2H-thiazolo[2,3-b]quinazoline-3,6(5H,7H)-dione(1287701-48-7)

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: 1287701-48-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1287701-48-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,8,7,7,0 and 1 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1287701-48:
(9*1)+(8*2)+(7*8)+(6*7)+(5*7)+(4*0)+(3*1)+(2*4)+(1*8)=177
177 % 10 = 7
So 1287701-48-7 is a valid CAS Registry Number.

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1287701-48-7Relevant academic research and scientific papers

Synthesis of some novel 2-arylidene thiazoloquinazolinone derivatives via one-pot, three-component reaction

Mobinikhaledi,Foroughifar,Ebrahimi,Rahimi,Zandi

, p. 457 - 463 (2011/05/15)

A one-pot, multicomponent reaction of thioxoquinazolinone with ethyl chloroacetate and aromatic aldehydes is described for the preparation of novel thiazoloquinazolinone derivatives using sodium hydride in ethanol under reflux conditions. The structures of all synthesized compounds were identified by IR, 1H NMR, 13C NMR, and elemental analysis data. Copyright Taylor & Francis Group, LLC.

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