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360-11-2

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360-11-2 Usage

Synthesis Reference(s)

Journal of the American Chemical Society, 109, p. 896, 1987 DOI: 10.1021/ja00237a043Tetrahedron, 27, p. 3965, 1971 DOI: 10.1016/S0040-4020(01)98258-4

Check Digit Verification of cas no

The CAS Registry Mumber 360-11-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,6 and 0 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 360-11:
(5*3)+(4*6)+(3*0)+(2*1)+(1*1)=42
42 % 10 = 2
So 360-11-2 is a valid CAS Registry Number.

360-11-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name [difluoro(phenyl)methyl]benzene

1.2 Other means of identification

Product number -
Other names (difluorophenylmethyl)benzene

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:360-11-2 SDS

360-11-2Relevant articles and documents

Alkali Metal Fluorides in Fluorinated Alcohols: Fundamental Properties and Applications to Electrochemical Fluorination

Shida, Naoki,Takenaka, Hiroaki,Gotou, Akihiro,Isogai, Tomohiro,Yamauchi, Akiyoshi,Kishikawa, Yosuke,Nagata, Yuuya,Tomita, Ikuyoshi,Fuchigami, Toshio,Inagi, Shinsuke

, p. 16128 - 16133 (2021/07/26)

Fundamental properties of alkali metal fluorides (MF, M = Cs, K) dissolved in 1,1,1,3,3,3-hexafluoroisopropanol (HFIP) or in 3,3,3-trifluoroethanol (TFE) are investigated, including solubility, conductivity, and viscosity. Solid-state structures of single crystals obtained from CsF/HFIP and CsF/TFE are described for the first time, giving insights into the multiple interactions between fluorinated alcohols and CsF. Applications in electrochemical fluorination reactions are successfully demonstrated.

Pd-Catalyzed Transfer of Difluorocarbene for Three Component Cross-Coupling?

Xu, Zhi-Wei,Zhang, Wei,Lin, Jin-Hong,Jin, Chuan-Ming,Xiao, Ji-Chang

supporting information, p. 1647 - 1650 (2020/10/19)

Outstanding accomplishments have been achieved in the chemistry of difluorocarbene, but transition- metal-catalyzed transfer of difluorocarbene for coupling remains a challenging task. Herein, we describe a Pd-catalyzed coupling of difluorocarbene with two aryl carbon centers to give difluoromethylenation products, which cannot be obtained by any previous difluorocarbene-transformation method.

DIFLUOROMETHYL AND DIFLUOROMETHYLENE TRANSFER REAGENTS

-

Paragraph 0022; 0096, (2020/01/22)

Disclosed herein are borazine, borate, and azaborinine compounds and compositions, methods of making said compounds and compositions, and methods of forming aromatic difluorocarbon compounds and difluorocarbon compounds.

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