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2a,7[1',2']:8,12b[1'',2'']-Dibenzenodibenzo[a,e]cyclobuta[c]cyclooctene,1,2,7,8-tetrahydro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

17277-99-5

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17277-99-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17277-99-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,2,7 and 7 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 17277-99:
(7*1)+(6*7)+(5*2)+(4*7)+(3*7)+(2*9)+(1*9)=135
135 % 10 = 5
So 17277-99-5 is a valid CAS Registry Number.

17277-99-5SDS

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 1,2,7,8-tetrahydro-2a,7[1',2']:8,12b[1'',2'']-dibezenodibenzo[a,e]cyclobuta[c]cyclooctene

1.2 Other means of identification

Product number -
Other names 1,2,7,8-Tetrahydro-2a,7,8,12b-di-o-benzeno-dibenzo[a,e]cyclobuta[c]cycloocten

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:17277-99-5 SDS

17277-99-5Downstream Products

17277-99-5Relevant academic research and scientific papers

Effect of substituents on the fluorescence quenching of a few (anthracen-9-yl)methanamines

Haridas, Suja,Jacob, Jomon P.,Mallia, Rekha R.,Mathew, Rani

, (2020)

This article deals with the photophysical properties of a few (anthracen-9-yl)methanamines. Analysis of absorption and the fluorescence emission spectra of these compounds indicated intramolecular photoinduced electron transfer leading to quenching of excited states, the efficiency of which depends on the geometrical constraints and electronic factors pertaining to the molecule. The decay kinetics studied using Time Correlated Single Photon Counting showed a bi-exponential decay indicating the involvement of two transient species in the excited state of these molecules. Also, we build up a relation between the rate of the photochemical reaction, free energy change and quenching of excited states.

Flash Pyrolysis of Selenides. Syntheses of Bibenzyls, Olefins, and Related Compounds

Higuchi, Hiroyuki,Otsubo, Tetsuo,Ogura, Fumio,Yamaguchi, Hachiro,Sakata, Yoshiteru,Misumi, Soichi

, p. 182 - 187 (2007/10/02)

Pyrolyses of a series of selenides and diselenides were studied. Selenides and diselenides bound with an active methylene group like benzyl gave a variety of substituted bibenzyls and related ethane derivatives in high yields. Other diselenides were easily caused to cleave to give various aromatic and aliphatic olefins in good yields together with elemental selenium. Lepidopterene, paracyclophane, and benzocyclobutene were prepared by thermal cleavage of their corresponding phenylselenomethyl-substituted compounds as an application of the pyrolysis concerned.

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