Cas 1055993-48-0,ethyl 6,7,8,9-tetrahydro-5-oxo-2-phenyl-1-(phenylsulfonyl)pyrrolo[2,1-b]thieno[2,3-b][1,3]oxazine-3-carboxylate

1055993-48-0

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Basic information

Product Name: ethyl 6,7,8,9-tetrahydro-5-oxo-2-phenyl-1-(phenylsulfonyl)pyrrolo[2,1-b]thieno[2,3-b][1,3]oxazine-3-carboxylate
Synonyms:
CAS NO:1055993-48-0
Molecular Formula:
Molecular Weight: 533.626
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: ethyl 6,7,8,9-tetrahydro-5-oxo-2-phenyl-1-(phenylsulfonyl)pyrrolo[2,1-b]thieno[2,3-b][1,3]oxazine-3-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 6,7,8,9-tetrahydro-5-oxo-2-phenyl-1-(phenylsulfonyl)pyrrolo[2,1-b]thieno[2,3-b][1,3]oxazine-3-carboxylate(1055993-48-0)
EPA Substance Registry System: ethyl 6,7,8,9-tetrahydro-5-oxo-2-phenyl-1-(phenylsulfonyl)pyrrolo[2,1-b]thieno[2,3-b][1,3]oxazine-3-carboxylate(1055993-48-0)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1055993-48-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1055993-48-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,5,5,9,9 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1055993-48:
(9*1)+(8*0)+(7*5)+(6*5)+(5*9)+(4*9)+(3*3)+(2*4)+(1*8)=180
180 % 10 = 0
So 1055993-48-0 is a valid CAS Registry Number.

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1055993-48-0Relevant academic research and scientific papers

Studies with phenylsulfone derivatives: Synthesis of pyrrole, thiophene and their fused derivatives

Elkholy, Yehya M.

, p. 1237 - 1241 (2008/12/20)

(Chemical Equation Presented) Diethyl 2-(1-phenyl-2-(phenylsulfonyl) ethylidene)malonate 3 has been prepared via the reaction of 6 with sodium benzenesulfinate. Compound 3 proved to be highly reactive towards various reagents and underwent numerous chemical transformation, resulting in the construction of a wide range of heterocyclic sulfone systems.

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