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28114-92-3

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28114-92-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 28114-92-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,1,1 and 4 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 28114-92:
(7*2)+(6*8)+(5*1)+(4*1)+(3*4)+(2*9)+(1*2)=103
103 % 10 = 3
So 28114-92-3 is a valid CAS Registry Number.

28114-92-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-phenylsulfanyl-9H-fluorene

1.2 Other means of identification

Product number -
Other names 9H-Fluorene,9-(phenylthio)

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:28114-92-3 SDS

28114-92-3Relevant articles and documents

Strain-Modulated Reactivity: An Acidic Silane

Tretiakov, Serhii,Witteman, Léon,Lutz, Martin,Moret, Marc-Etienne

, p. 9618 - 9626 (2021)

Compounds of main-group elements such as silicon are attractive candidates for green and inexpensive catalysts. For them to compete with state-of-the-art transition-metal complexes, new reactivity modes must be unlocked and controlled, which can be achiev

Base-Promoted Oxidative C(sp3)–S Bond Cross-Coupling of Inactive Fluorenes and Thiols for the Synthesis of 9-Monothiolated Fluorenes

Liu, Yafeng,Yuan, Xinglong,Su, Kexin,Tian, Yuan,Chen, Baohua

supporting information, p. 1649 - 1652 (2019/01/30)

The highly efficient and selective C(sp3)–S bond cross-coupling method for the synthesis of 9-thiolated fluorenes through a direct thiolation at 9-C(sp3)–H of fluorenes with thiols is described. This reaction occurs at ambient conditions and shows good tolerance of functional groups including arylthiols and alkylthiols. A wide range of products is obtained in moderate to good yields. Besides, the reaction of benzothiophenol and fluorine generates unexpected 9-benzylidene-9H-fluorene by eliminating hydrogen sulfide.

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