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138321-99-0

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  • 6fapbp 4,4'-Bis(4-amino-2-trifluoromethylphenoxy)biphenyl Manufacturer Factory CAS 138321-99-0

    Cas No: 138321-99-0

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  • 4-[4-[4-[4-amino-2-(trifluoromethyl)phenoxy]phenyl]phenoxy]-3-(trifluoromethyl)aniline

    Cas No: 138321-99-0

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138321-99-0 Usage

General Description

6FAPBP, or 6-(2-Fluorophenyl)-1-benzofuran-3-yl)(2,2,3,3-tetramethylcyclopropyl)methanone, is a synthetic cannabinoid that acts as a potent agonist for the cannabinoid receptors. It is a research chemical that is structurally related to the synthetic cannabinoid MDMB-CHMICA, and it has been found to have similar effects on the central nervous system. 6FAPBP is known for its strong psychoactive effects, including euphoria, relaxation, and altered perception of time and space. It is often used in scientific research to study the effects of synthetic cannabinoids on the brain and behavior. However, 6FAPBP is not approved for human consumption and is considered a dangerous and potentially harmful substance.

Check Digit Verification of cas no

The CAS Registry Mumber 138321-99-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,3,2 and 1 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 138321-99:
(8*1)+(7*3)+(6*8)+(5*3)+(4*2)+(3*1)+(2*9)+(1*9)=130
130 % 10 = 0
So 138321-99-0 is a valid CAS Registry Number.

138321-99-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[4-[4-[4-amino-2-(trifluoromethyl)phenoxy]phenyl]phenoxy]-3-(trifluoromethyl)aniline

1.2 Other means of identification

Product number -
Other names 4,4'-BIS(4-AMINO-2-TRIFLUOROMETHYLPHENOXY)BIPHENYL

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:138321-99-0 SDS

138321-99-0Downstream Products

138321-99-0Relevant articles and documents

Synthesis and characterization of sulfonated polyimides containing trifluoromethyl groups as proton exchange membranes

Zhang, Qingshuang,Li, Qiaoling

, p. 1460 - 1466 (2011)

A novel sulfonated diamine, 4,4′-bis(4-amino-3- trifluoromethylphenoxy) biphenyl 3,3′-disulfonic acid (F-BAPBDS), was successfully synthesized by nucleophilic aromatic substitution of 4,4′-dihydroxybiphenyl with 2-chloro-5-nitrobenzotrifluoride, followed by reduction and sulfonation. A series of sulfonated polyimides of high molecular weight (SPI-x, x represents the molar percentage of the sulfonated monomer) were prepared by copolymerization of 1,4,5,8-naphathlenetetracarboxylic dianhydride (NTDA) with F-BAPBDS and nonsulfonated diamine. Flexible and tough membranes of high mechanical strength were obtained by solution casting and the electrolyte properties of the polymers were intensively investigated. The copolymer membranes exhibited excellent oxidative stability due to the introducing of the CF3 groups. The SPI membranes displayed desirable proton conductivity (0.52 × 10-1-0.97 × 10-1 S·cm -1) and low methanol permeability (less than 2.8 × 10 -7 cm2·s-1). The highest proton conductivity (1.89 × 10-1 S·cm-1) was obtained for the SPI-90 membrane at 80°C, with an IEC of 2.12 mequiv/g. This value is higher than that of Nafion 117 (1.7 × 10-1 S·cm-1). Furthermore, the hydrolytic stability of the obtained SPIs is better than the BDSA and ODADS based SPIs due to the hydrophobic CF3 groups which protect the imide ring from being attacked by water molecules, in spite of its strong electron-withdrawing behaviors. Copyright

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