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9,10-dimethyl-9,10-dihydro-9,10-epidioxyanthracene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

14923-28-5

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14923-28-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14923-28-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,9,2 and 3 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 14923-28:
(7*1)+(6*4)+(5*9)+(4*2)+(3*3)+(2*2)+(1*8)=105
105 % 10 = 5
So 14923-28-5 is a valid CAS Registry Number.

14923-28-5SDS

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-dimethyl-9,10-dioxatricyclo[6.6.2.02,7]anthracene

1.2 Other means of identification

Product number -
Other names 9,10-Dimethyl-9,10-anthracen-endo-peroxid

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:14923-28-5 SDS

14923-28-5Downstream Products

14923-28-5Relevant academic research and scientific papers

Iodosylbenzene Coordination Chemistry Relevant to Metal-Organic Framework Catalysis

Cardenal, Ashley D.,Maity, Asim,Gao, Wen-Yang,Ashirov, Rahym,Hyun, Sung-Min,Powers, David C.

, p. 10543 - 10553 (2019/09/13)

Hypervalent iodine compounds formally feature expanded valence shells at iodine. These reagents are broadly used in synthetic chemistry due to the ability to participate in well-defined oxidation-reduction processes and because the ligand-exchange chemist

Titanium tetra-tert-butoxide-tert-butyl hydroperoxide oxidizing system: Physicochemical and chemical aspects

Stepovik,Gulenova,Martynova,Mar'Yasin,Cherkasov

, p. 266 - 276 (2008/09/20)

The reaction of titanium tetra-tert-butoxide with tert-butyl hydroperoxide (1: 2) (C6H6, 20 C) involves the steps of formation of the titanium-containing peroxide (t-BuO)3TiOOBu-t and peroxytrioxide (t-BuO)3TiOOOBu-t. The latter decomposes with the release of oxygen, often in the singlet form, and also homolytically with cleavage of both peroxy bonds. The corresponding alkoxy and peroxy radicals were identified by ESR using spin traps. The title system oxidizes organic substrates under mild conditions. Depending on the substrate structure, the active oxidant species can be titanium-containing peroxide, peroxytrioxide, and oxygen generated by the system.

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