Cas 1383382-99-7,3-(4-methoxyphenyl)-3-phenyl-10,12-dibromo-6-trifluoromethyl-13,13-dimethyl-3H,13H-indeno[2',3':3,4]naphtho[1,2-b]pyran

1383382-99-7

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Basic information

Product Name: 3-(4-methoxyphenyl)-3-phenyl-10,12-dibromo-6-trifluoromethyl-13,13-dimethyl-3H,13H-indeno[2',3':3,4]naphtho[1,2-b]pyran
Synonyms: 3-(4-methoxyphenyl)-3-phenyl-10,12-dibromo-6-trifluoromethyl-13,13-dimethyl-3H,13H-indeno[2',3':3,4]naphtho[1,2-b]pyran
CAS NO:1383382-99-7
Molecular Formula:
Molecular Weight: 706.397
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: 3-(4-methoxyphenyl)-3-phenyl-10,12-dibromo-6-trifluoromethyl-13,13-dimethyl-3H,13H-indeno[2',3':3,4]naphtho[1,2-b]pyran(CAS DataBase Reference)
NIST Chemistry Reference: 3-(4-methoxyphenyl)-3-phenyl-10,12-dibromo-6-trifluoromethyl-13,13-dimethyl-3H,13H-indeno[2',3':3,4]naphtho[1,2-b]pyran(1383382-99-7)
EPA Substance Registry System: 3-(4-methoxyphenyl)-3-phenyl-10,12-dibromo-6-trifluoromethyl-13,13-dimethyl-3H,13H-indeno[2',3':3,4]naphtho[1,2-b]pyran(1383382-99-7)

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: 1383382-99-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1383382-99-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,3,3,8 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1383382-99:
(9*1)+(8*3)+(7*8)+(6*3)+(5*3)+(4*8)+(3*2)+(2*9)+(1*9)=187
187 % 10 = 7
So 1383382-99-7 is a valid CAS Registry Number.

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1383382-99-7Relevant academic research and scientific papers

LACTONE COMPOUNDS AND MATERIALS MADE THEREFROM

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, (2012/06/30)

The present invention relates to lactone compounds represented by the following Formulas I and II, and methods of making such lactone compounds. The present invention also relates to methods of making other materials from such lactone compounds, such as fused ring indenol compounds (e.g., indeno-fused naphthols), and fused ring indenopyran compounds (e.g., indeno-fused naphthopyrans).

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