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57028-28-1

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57028-28-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57028-28-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,0,2 and 8 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 57028-28:
(7*5)+(6*7)+(5*0)+(4*2)+(3*8)+(2*2)+(1*8)=121
121 % 10 = 1
So 57028-28-1 is a valid CAS Registry Number.

57028-28-1SDS

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-(4-methylphenyl)fluoren-9-ol

1.2 Other means of identification

Product number -
Other names 9-(4-methylphenyl)-9H-fluoren-9-ol

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:57028-28-1 SDS

57028-28-1Relevant articles and documents

A Sc(OTf)3 catalyzed dehydrogenative reaction of electron-rich (hetero)aryl nucleophiles with 9-aryl-fluoren-9-ols

Zhou, Chen,Hu, Chen,Hong, Gang,He, Yuchen,Tang, Zhicong,Wang, Limin

supporting information, p. 9615 - 9619 (2019/11/20)

A highly efficient dehydrogenative reaction of a series of nucleophiles with 9-aryl-fluoren-9-ols has been realized by using only 2 mol% of Sc(OTf)3 as a catalyst. The corresponding indole-containing 9,9-diarylfluorenes were obtained in up to 99% yield as well as other electron-rich (hetero)arene adducts. The protocol exhibits high selectivity, mild reaction conditions and good substrate compatibility (32 examples). This protocol is further highlighted by its applications in the construction of potential electroluminescent materials.

Direct C-H bond arylation of fluorenes with aryl chlorides catalyzed by N-heterocyclic carbene-palladium(ii)-1-methylimidazole complex and further transformation of the products in a one-pot procedure

Ji, Ya-Yun,Lu, Li-Li,Shi, Yu-Chun,Shao, Li-Xiong

, p. 8488 - 8498 (2014/12/10)

We report here the NHC-Pd(ii)-Im complex 1-catalyzed direct C-H bond functionalization of the C9 position of fluorenes with aryl chlorides and further transformation of the resulting products in a one-pot procedure. Under the optimal conditions, arylated fluorenes can be obtained in moderate to almost quantitative yields using various activated and unactivated (hetero)aryl chlorides as the arylating reagents. Furthermore, if the mixture from the arylation reaction is exposed to air, the C9-oxidized products can be obtained in acceptable to good yields in a one-pot procedure. In addition, alkyl groups can also be efficiently introduced to the above mixture from the arylation reaction, producing further C9-alkylated products in good to almost quantitative yields in a one-pot procedure, thus providing an expedient, inexpensive and practical strategy for the mono- and di-functionalization of fluorenes. This journal is

The construction of H-shaped fluorescent materials based on building blocks consisting of triphenylamine and fluorene

Zhang, Cheng,Zhang, Yu-Jian,Xiang, Wen-Qin,Hu, Bin,Ouyang, Mi,Xu, Yi,Ma, Chun-An

supporting information; experimental part, p. 520 - 521 (2010/09/05)

A class of complicated 9,9-diarylfluorenes as nonplanar building blocks were synthesized and utilized to prepare a novel H-shaped oligofluorene. High glass transition temperatures and excellent solubility of the obtained oligomers indicated the 9,9diarylfluorenes would be promising building blocks for the construction of H-shaped optoelectronic materials.

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