Cas 86149-04-4,p-Tolyloxy-thioacetic acid S-[6,8-dibromo-3-(4-chloro-phenyl)-4-oxo-3,4-dihydro-quinazolin-2-yl] ester

86149-04-4

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Basic information

Product Name: p-Tolyloxy-thioacetic acid S-[6,8-dibromo-3-(4-chloro-phenyl)-4-oxo-3,4-dihydro-quinazolin-2-yl] ester
Synonyms: p-Tolyloxy-thioacetic acid S-[6,8-dibromo-3-(4-chloro-phenyl)-4-oxo-3,4-dihydro-quinazolin-2-yl] ester
CAS NO:86149-04-4
Molecular Formula:
Molecular Weight: 594.711
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: p-Tolyloxy-thioacetic acid S-[6,8-dibromo-3-(4-chloro-phenyl)-4-oxo-3,4-dihydro-quinazolin-2-yl] ester(CAS DataBase Reference)
NIST Chemistry Reference: p-Tolyloxy-thioacetic acid S-[6,8-dibromo-3-(4-chloro-phenyl)-4-oxo-3,4-dihydro-quinazolin-2-yl] ester(86149-04-4)
EPA Substance Registry System: p-Tolyloxy-thioacetic acid S-[6,8-dibromo-3-(4-chloro-phenyl)-4-oxo-3,4-dihydro-quinazolin-2-yl] ester(86149-04-4)

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: 86149-04-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 86149-04-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,1,4 and 9 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 86149-04:
(7*8)+(6*6)+(5*1)+(4*4)+(3*9)+(2*0)+(1*4)=144
144 % 10 = 4
So 86149-04-4 is a valid CAS Registry Number.

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86149-04-4Relevant academic research and scientific papers

Synthesis of some new 2-(phenoxyacetylthio)-3-aryl-6-bromo- or 6,8-dibromoquinazoline-4(3H)-ones as possible AChE inhibitors

Hajela Km.,Sengupta,Shanker,Doval

, p. 431 - 434 (2007/10/02)

Sixteen new 2-(phenoxyacetylthio)-3-aryl-6-bromo- or -6,8-dibromoquinazolines were synthesized by condensation of various phenoxyacetyl chlorides with mercaptoquinazolines. Their inhibitory properties towards choline esterase and their bactericidal activities were studied in vitro. Nine of the compounds exhibited (>50%) choline esterase inhibition, whereas the antibacterial screening showed moderate results.

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