Cas 1218784-29-2,N-phthalimidyl [2-phenyl-4-oxo-3-[{2-oxo-2-(phenothiazin-10-yl)ethyl}amino]-1,3-thiazolidin-5-yl]ethanoate

1218784-29-2

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Basic information

Product Name: N-phthalimidyl [2-phenyl-4-oxo-3-[{2-oxo-2-(phenothiazin-10-yl)ethyl}amino]-1,3-thiazolidin-5-yl]ethanoate
Synonyms:
CAS NO:1218784-29-2
Molecular Formula:
Molecular Weight: 636.709
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-phthalimidyl [2-phenyl-4-oxo-3-[{2-oxo-2-(phenothiazin-10-yl)ethyl}amino]-1,3-thiazolidin-5-yl]ethanoate(CAS DataBase Reference)
NIST Chemistry Reference: N-phthalimidyl [2-phenyl-4-oxo-3-[{2-oxo-2-(phenothiazin-10-yl)ethyl}amino]-1,3-thiazolidin-5-yl]ethanoate(1218784-29-2)
EPA Substance Registry System: N-phthalimidyl [2-phenyl-4-oxo-3-[{2-oxo-2-(phenothiazin-10-yl)ethyl}amino]-1,3-thiazolidin-5-yl]ethanoate(1218784-29-2)

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: 1218784-29-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1218784-29-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,8,7,8 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1218784-29:
(9*1)+(8*2)+(7*1)+(6*8)+(5*7)+(4*8)+(3*4)+(2*2)+(1*9)=172
172 % 10 = 2
So 1218784-29-2 is a valid CAS Registry Number.

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1218784-29-2Relevant academic research and scientific papers

Synthesis of phthalimido or succinimido-[2-aryl-4-oxo-3-[{2-oxo-2- (phcnothiazin-10-yl)ethyl}amino]-1,3-thiazolidin-5-yl]ethanoate and their antimicrobial activities

Salvi, Vijay Kumar,Sharma, Shweta,Sharma, Chirag,Bhambi, Dinesh,Talesara

experimental part, p. 1583 - 1589 (2010/03/24)

Keeping in view the pharmacological potential of thiazolidinones and phenothiazines, the title compounds containing these nuclei have been synthesized. Reaction of 10-(chloroacclyl)phcnolhiazinc 1 with hydrazine hydrate gives 10(hydrazinoacetyl)phenothiaz

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