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15088-28-5

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15088-28-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15088-28-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,0,8 and 8 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 15088-28:
(7*1)+(6*5)+(5*0)+(4*8)+(3*8)+(2*2)+(1*8)=105
105 % 10 = 5
So 15088-28-5 is a valid CAS Registry Number.

15088-28-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-N,1-N,4-N,4-N-tetraphenylbenzene-1,4-dicarboxamide

1.2 Other means of identification

Product number -
Other names tetra-N-phenyl-terephthalamide

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:15088-28-5 SDS

15088-28-5Downstream Products

15088-28-5Relevant articles and documents

Excited-state conformation capture by supramolecular chains towards triplet-involved organic emitters

Liu, Hao,Ando, Naoki,Yamaguchi, Shigehiro,Naumov, Pan?e,Zhang, Hongyu

supporting information, p. 1669 - 1674 (2021/03/08)

Nowadays, the development of triplet-involved materials becomes a hot research topic in solid-state luminescence fields. However, the mechanism of triplet-involved emission still remains some mysteries to conquer. Here, we proposed a new concept of excited-state conformation capture for the constructions of different types of triplet-involved materials. Firstly, excited-state conformation could be trapped by supramolecular chains in crystal and form a new optimum excited-state structure which is different from that in solution or simple rigid environment, leading to bright thermally activated delayed fluorescence (TADF) emission. Based on excited-state conformation capture methodology, next, we obtained room-temperature phosphorescence (RTP) by introducing Br atoms for the enhancement of intersystem crossing. It could be concluded from experimental results that TADF may originate from aggregate effect while RTP may derive from monomers. Finally, heavy-atom free RTP and ultra RTP were achieved by eliminating aggregate effect. This work could not only extend the design methodology of triplet-involved materials but also set clear evidences for the mechanism of triplet-involved emissions.

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