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6267-02-3

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6267-02-3 Usage

Chemical Properties

Dark brown viscous body

Check Digit Verification of cas no

The CAS Registry Mumber 6267-02-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,6 and 7 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6267-02:
(6*6)+(5*2)+(4*6)+(3*7)+(2*0)+(1*2)=93
93 % 10 = 3
So 6267-02-3 is a valid CAS Registry Number.
InChI:InChI=1/C15H15N/c1-15(2)11-7-3-5-9-13(11)16-14-10-6-4-8-12(14)15/h3-10,16H,1-2H3

6267-02-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 9,10-Dihydro-9,9-dimethylacridine

1.2 Other means of identification

Product number -
Other names 9,10-dihydro-9,9-dimethyl-acridin

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:6267-02-3 SDS

6267-02-3Relevant articles and documents

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Taylor,Procter

, p. 2537 (1971)

-

Deuterated organic compounds for organic light-emitting diode and organic light-emitting diode including the same

-

, (2020/12/15)

The present invention relates to an organic electroluminescent compound represented by chemical formula A and an organic light emitting device comprising the same. Substituents Y, Ar2 , L3 , K, p and x are as defined in the description of the invention. [Chemical A] (by machine translation)

New reductive rearrangement of: N-arylindoles triggered by the grubbs-stoltz reagent et3sih/kotbu

Allison, Mark,Arokianathar, Jude N.,Dimitrova, Daniela,Kolodziejczak, Krystian,Leach, Stuart G.,Murphy, John A.,Parkinson, John A.,Poole, Darren L.,Smith, Andrew J.,Tuttle, Tell,Young, Allan

, p. 3719 - 3726 (2020/04/20)

N-Arylindoles are transformed into dihydroacridines in a new type of rearrangement, through heating with triethylsilane and potassium tert-butoxide. Studies indicate that the pathway involves (i) the formation of indole radical anions followed by fragmentation of the indole C2-N bond, and (ii) a ring-closing reaction that follows a potassium-ion dependent hydrogen atom transfer step. Unexpected behaviors of 'radical-trap' substrates prove very helpful in framing the proposed mechanism.

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