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9-tert-Butyl-9,10-(dewar anthracene) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

76008-29-2

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76008-29-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76008-29-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,0,0 and 8 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 76008-29:
(7*7)+(6*6)+(5*0)+(4*0)+(3*8)+(2*2)+(1*9)=122
122 % 10 = 2
So 76008-29-2 is a valid CAS Registry Number.

76008-29-2SDS

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-tert-Butyl-9,10-(dewar anthracene)

1.2 Other means of identification

Product number -
Other names 9-t-Butyl-9,10-dewaranthrazen

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:76008-29-2 SDS

76008-29-2Upstream product

76008-29-2Downstream Products

76008-29-2Relevant academic research and scientific papers

Rotation mobility of the guest molecules and its reactivity in the thermal reaction in the solid matrix

Minaylov,Vorobiev,Gurman

, p. 97 - 101 (1994)

Characteristic times of the thermal reaction and the molecular rotation for the guest molecules have been measured in polystyrene films. Rotation mobility of molecules was determined from the relaxation of the light induced optical anisotropy of the photoselected samples. Close agreement of the activation energies and characteristic times of thermal reaction and molecular rotation was observed. By the comparison of the induced optical anisotropy of the initial and photoconverted molecules the angles of the rotation of the molecular dipole transition moment in the instant of the elementary act of the photochemical conversion were determined.

Photochemical Valence Isomerization of 9-alkyl-substituted Anthracenes to 9,10-Dewarisomers.

Jahn,Dreeskamp

, p. 42 - 47 (2007/10/02)

On light absorption in the long wavelength **1L//a-band 9-alkyl-substituted anthracenes in fluid solutions isomerize with low quantum yield (about 0. 016 at 300 K) to the 9,10-Dewarisomer, provided the substituent is sufficiently spacefilling (t-butyl or t-pentyl). On increasing the viscosity and/or reducing the temperature the quantum yield of this valence isomerization decreases while the quantum yield of fluorescence and the vibrational structure of the fluorescence emission increases. From spectroscopic, caloric and kinetic data an energy diagram of the ground and first excited states is constructed for this photo- and thermoreversible reaction in which the folding along the 9,10-axis of the anthracene sceleton serves as the main reaction coordinate.

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