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714972-01-7

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714972-01-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 714972-01-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,1,4,9,7 and 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 714972-01:
(8*7)+(7*1)+(6*4)+(5*9)+(4*7)+(3*2)+(2*0)+(1*1)=167
167 % 10 = 7
So 714972-01-7 is a valid CAS Registry Number.

714972-01-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-fluoro-9H-xanthene

1.2 Other means of identification

Product number -
Other names 9H-Xanthene,2-fluoro

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:714972-01-7 SDS

714972-01-7Downstream Products

714972-01-7Relevant articles and documents

Electrochemically Mediated Direct C(sp3)?H Sulfonylation of Xanthene Derivatives

Wei, Wan-Jie,Zhong, Yu-Jing,Feng, Yu-Feng,Gao, Lei,Tang, Hai-Tao,Pan, Ying-Ming,Ma, Xian-Li,Mo, Zu-Yu

supporting information, p. 726 - 731 (2022/01/06)

The construction of C(sp3)-sulfonyl bonds through direct sulfonylation of C(sp3)?H bond presents a number of challenges, so an electrochemical oxidation-induced direct sulfonylation of the xanthene C(sp3)?H bond was developed. Significant advantages of this method are high atom efficiency, functional group tolerance, transition metal- and oxidant-free conditions. The in vitro cytotoxicity of all product is evaluated by MTT assay against human cancer cell lines. The results reveal that most of the compounds 3 da and 3 af have good inhibitory activity on tumor cell lines. (Figure presented.).

Copper-Catalyzed One-Pot Synthesis of Dibenzofurans, Xanthenes, and Xanthones from Cyclic Diphenyl Iodoniums

Zhu, Daqian,Li, Min,Wu, Zhouming,Du, Yongliang,Luo, Bingling,Huang, Peng,Wen, Shijun

, p. 4566 - 4571 (2019/07/09)

Oxygenation of cyclic diphenyl iodoniums (CDPIs) with varied medium-ring sizes has been fully investigated. This practical copper-catalyzed tandem reaction of CDPIs with water as the oxygen source enables the construction of derivatised dibenzofurans and xanthenes at moderate to good yields. Moreover, structurally important xanthones are also successfully accessed under the oxygenation conditions with additional TEMPO.

Oxazoles as mGluR 1 enhancers

-

Page/Page column 6, (2010/02/07)

The invention relates to carboxamide derivatives as defined in the specification and claims, to a process for their preparation, to pharmaceutical compositions comprising them and to their use as mGluR1 enhancers in the treatment and prevention of neurological disorders and diseases, such as Alzheimer's disease and dementia.

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