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89346-58-7

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89346-58-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89346-58-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,3,4 and 6 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 89346-58:
(7*8)+(6*9)+(5*3)+(4*4)+(3*6)+(2*5)+(1*8)=177
177 % 10 = 7
So 89346-58-7 is a valid CAS Registry Number.

89346-58-7SDS

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 2-(4-chlorophenyl)benzonitrile

1.2 Other means of identification

Product number -
Other names 4'-chlorobiphenyl-2-carbonitrile

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:89346-58-7 SDS

89346-58-7Relevant articles and documents

Synthesis of highly substituted fluorenones via metal-free TBHP-promoted oxidative cyclization of 2-(aminomethyl)biphenyls. Application to the total synthesis of nobilone

Bracher, Franz,Jourjine, Ilya A. P.,Krau?, Jürgen,Zeisel, Lukas

supporting information, p. 2668 - 2679 (2021/11/30)

Highly substituted fluorenones are readily prepared in mostly fair to good yields via metal- and additive-free TBHP-promoted cross-dehydrogenative coupling (CDC) of readily accessible N-methyl-2-(aminomethyl)biphenyls and 2-(aminomethyl)biphenyls. This methodology is compatible with numerous functional groups (methoxy, cyano, nitro, chloro, and SEM and TBS-protective groups for phenols) and was further utilized in the first total synthesis of the natural product nobilone.

High-performance sky-blue phosphorescent organic light-emitting diodes employing wide-bandgap bipolar host materials with thermally activated delayed fluorescence characteristics

Zhang, Yuan-Lan,Ran, Quan,Wang, Qiang,Tian, Qi-Sheng,Kong, Fan-Cheng,Fan, Jian,Liao, Liang-Sheng

, (2020/03/03)

Up to date, several kinds of thermally activated delayed fluorescence (TADF) host molecules have been rapidly developed to fulfill the increasing demand of high-efficiency phosphorescent organic light-emitting diodes (PHOLEDs). Herein, three wide-bandgap TADF materials BPCN-Cz2Ph, BPCN-2Cz, and BPCN-3Cz are newly designed and synthesized as host materials for sky-blue PHOLEDs. By modulation of carbazole-units in the molecular skeleton, we find that the optimized molecules can realize both high triplet energies and balanced carrier transport properties with obvious TADF properties. The sky-blue PHOLEDs with ultralow phosphor doping ratio employing BPCN-Cz2Ph, BPCN-2Cz, and BPCN-3Cz as host materials demonstrate really high performance with alleviated roll-offs and achieve impressive current efficiencies (CEs) of 46.5 cd A?1, 50.0 cd A?1, and 34.5 cd A?1, power efficiencies (PEs) of 40.6 lm W?1, 46.8 lm W?1, and 34.8 lm W?1, and external quantum efficiencies (EQEs) of 22.2%, 24%, and 15.8%, respectively. More encouragingly, even at an applied luminance of 1000 cd m?2, the EQEs could maintain high levels of 21.0%, 21.5% and 12.8%, respectively, which represents the potential utility value of the new family of these molecules in blue PHOLEDs. Our molecular design strategy provides a practical way to construct promising wide-bandgap TADF host materials with an excellent combination of TADF property, high triplet energy, and balanced carrier-transporting ability for high-performance devices.

Process for synthesizing boscalid

-

Paragraph 0061-0064, (2019/05/02)

The invention discloses a process for synthesizing boscalid. The process comprises the following steps: (1) coupling o-chlorobenzonitrile with benzene to obtain 2-cyanobiphenyl, then carrying out chlorination, reduction and salt formation purification to obtain 4'-chloro-2-aminobiphenyl hydrochloride; (2) carrying out condensation reaction on the prepared 4'-chloro-2-aminobiphenyl hydrochloride and 2-chloronicotinoyl chloride to obtain the boscalid. The process for synthesizing the boscalid has the advantages of simple synthesis process, no need of complex aftertreatment, cheap and easily available basic chemical raw materials, and suitability for industrial production.

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