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17825-40-0

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17825-40-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17825-40-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,8,2 and 5 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 17825-40:
(7*1)+(6*7)+(5*8)+(4*2)+(3*5)+(2*4)+(1*0)=120
120 % 10 = 0
So 17825-40-0 is a valid CAS Registry Number.

17825-40-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4,5,6-tetramethylphenanthrene-9,10-dione

1.2 Other means of identification

Product number -
Other names phenantrene orthoquinone

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:17825-40-0 SDS

17825-40-0Downstream Products

17825-40-0Relevant articles and documents

Syntheses, Enrichment of Enantiomers, and Barriers to Racemization of Twisted 9,10-Phenanthrenquinones

Fritsch, Rainer,Hartmann, Erwin,Andert, Doris,Mannschreck, Albrecht

, p. 849 - 856 (2007/10/02)

The known syntheses of the 9,10-phenanthrenequinones 10a-c were improved by the chlorotrimethylsilane modification of the acyloin condensation of biaryl diesters.The novel quinones 4a, 4b, and 12 were prepared.For the first time, enantiomers (M and P) of this class of compounds were enriched semipreparatively by liquid chromatography on optically active sorbents.The barriers to thermal racemization amount to 90-130 kJ mol-1 (Table 2) and are thus higher than the barriers for the corresponding phenanthrene hydrocarbons by roughly 20 kJ mol -1.The reasons for this increase are discussed in terms of repulsive interactions in the trans ition state of helix inversion.

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