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1,10-diphenyldeca-1,9-diyne-3,8-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

77267-31-3

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77267-31-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77267-31-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,2,6 and 7 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 77267-31:
(7*7)+(6*7)+(5*2)+(4*6)+(3*7)+(2*3)+(1*1)=153
153 % 10 = 3
So 77267-31-3 is a valid CAS Registry Number.

77267-31-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,10-diphenyldeca-1,9-diyne-3,8-dione

1.2 Other means of identification

Product number -
Other names 1,10-Diphenyl-1,9-decadiyne-3,8-dione

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:77267-31-3 SDS

77267-31-3Relevant academic research and scientific papers

The Photo-Dehydro-Diels-Alder (PDDA) reaction - A powerful method for the preparation of biaryls

Wessig, Pablo,Mueller, Gunnar,Pick, Charlotte,Matthes, Annika

, p. 464 - 477 (2007/12/27)

The photochemically initiated dehydro-Diels-Alder (PDDA) reaction is an efficient and versatile method for the preparation of biaryls. The ring closure may take place both inter- and intramolecularly, of which the intramolecular variant is more productive

The photo-dehydro-diels-alder reaction: An efficient route to naphthalenes

Wessig, Pablo,Mueller, Gunnar,Kuehn, Andreas,Herre, Robert,Blumenthal, Haiko,Troelenberg, Stefanie

, p. 1445 - 1454 (2007/10/03)

The photo-dehydro-Diels-Alder reaction (PDDA), a new photochemical route to naphthalenes is presented. The [4+2] cycloaddition takes place between 3-arylynones and arylacetylenes. in which these moieties may be located in two molecules (intermolecular PDD

Synthesis and protein degradation capacity of photoactivated enediynes

Fouad, Farid S.,Wright, Justin M.,Plourde II, Gary,Purohit, Ajay D.,Wyatt, Justin K.,El-Shafey, Ahmed,Hynd, George,Crasto, Curtis F.,Lin, Yiqing,Jones, Graham B.

, p. 9789 - 9797 (2007/10/03)

The viability of proteins as targets of thermally and photoactivated enediynes has been confirmed at the molecular level. Model studies using a labeled substrate confirmed the efficacy of atom transfer from diyl radicals produced from enediynes to form captodatively stabilized carbon centered aminoacyl radicals, which then undergo either fragmentation or dimerization. To exploit this finding, a family of enediynes was developed using an intramolecular coupling strategy. Derivatives were prepared and used to target specific proteins, showing good correlation between affinity and photoinduced protein degrading activity. The findings have potential applications in the design of artificial chemical proteases and add to our understanding of the mechanism of action of the clinically important enediyne antitumor antibiotics.

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