Cas 98153-91-4,1,2,4-Triazolidine-3,5-dione, 1-[7,7a-dihydro-7a-(1-methylethyl)-1-oxo-1H-inden-7-yl]-4-phenyl-, trans-

98153-91-4

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Basic information

Product Name: 1,2,4-Triazolidine-3,5-dione, 1-[7,7a-dihydro-7a-(1-methylethyl)-1-oxo-1H-inden-7-yl]-4-phenyl-, trans-
Synonyms:
CAS NO:98153-91-4
Molecular Formula: C20H19N3O3
Molecular Weight: 349.389
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: 1,2,4-Triazolidine-3,5-dione, 1-[7,7a-dihydro-7a-(1-methylethyl)-1-oxo-1H-inden-7-yl]-4-phenyl-, trans-(CAS DataBase Reference)
NIST Chemistry Reference: 1,2,4-Triazolidine-3,5-dione, 1-[7,7a-dihydro-7a-(1-methylethyl)-1-oxo-1H-inden-7-yl]-4-phenyl-, trans-(98153-91-4)
EPA Substance Registry System: 1,2,4-Triazolidine-3,5-dione, 1-[7,7a-dihydro-7a-(1-methylethyl)-1-oxo-1H-inden-7-yl]-4-phenyl-, trans-(98153-91-4)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 98153-91-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 98153-91-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,1,5 and 3 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 98153-91:
(7*9)+(6*8)+(5*1)+(4*5)+(3*3)+(2*9)+(1*1)=164
164 % 10 = 4
So 98153-91-4 is a valid CAS Registry Number.

98153-91-4Upstream product

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98153-91-4Relevant academic research and scientific papers

3aH-Indenes. Part 5. Preparation and Reactions of 3-Methoxy- and 3-Trimethylsiloxy-3a-substituted-3aH-indenes

Gibbard, Howard C.,Moody, Christopher J.,Rees, Charles W.

, p. 723 - 730 (2007/10/02)

Previous work on the synthesis and cycloaddition of 3a-methyl-3aH-indenes (1a) and (1b) has been extended to substituents other than methyl at the ring junction.However, the increased migratory aptitudes of these substituents limits the scope of the 3aH-i

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