Cas 1447967-40-9,4-((3,6-dibromo-9H-carbazol-9-yl)methyl)-2-phenyl-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide

1447967-40-9

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Basic information

Product Name: 4-((3,6-dibromo-9H-carbazol-9-yl)methyl)-2-phenyl-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide
Synonyms: 4-((3,6-dibromo-9H-carbazol-9-yl)methyl)-2-phenyl-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide
CAS NO:1447967-40-9
Molecular Formula:
Molecular Weight: 612.341
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: 4-((3,6-dibromo-9H-carbazol-9-yl)methyl)-2-phenyl-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide(CAS DataBase Reference)
NIST Chemistry Reference: 4-((3,6-dibromo-9H-carbazol-9-yl)methyl)-2-phenyl-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide(1447967-40-9)
EPA Substance Registry System: 4-((3,6-dibromo-9H-carbazol-9-yl)methyl)-2-phenyl-3,4-dihydro-2H-benzo[b][1,4,5]oxathiazepine 1,1-dioxide(1447967-40-9)

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: 1447967-40-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1447967-40-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,7,9,6 and 7 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1447967-40:
(9*1)+(8*4)+(7*4)+(6*7)+(5*9)+(4*6)+(3*7)+(2*4)+(1*0)=209
209 % 10 = 9
So 1447967-40-9 is a valid CAS Registry Number.

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1447967-40-9Relevant academic research and scientific papers

Development of a scalable synthesis of P7C3-A20, a potent neuroprotective agent

Naidoo, Jacinth,Bemben, Christopher J.,Allwein, Shawn R.,Liang, Jue,Pieper, Andrew A.,Ready, Joseph M.

, p. 4429 - 4431 (2013/07/26)

A scalable synthesis of the neuroprotective agent P7C3-A20 is described. The synthesis has provided hundred-gram batches of the final compound for biological evaluation in rodents primates. The synthesis can be performed without chromatographic purificati

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