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Acetamide, N,N'-1,5-pentanediylbis[2,2,2-trifluoro-, also known as 1,5-Pentanediylbis(2,2,2-trifluoroacetamide), is a chemical compound with the molecular formula C9H10F6N2O2. It is a white crystalline solid that is soluble in organic solvents. Acetamide, N,N'-1,5-pentanediylbis[2,2,2-trifluoro- is primarily used as a reagent in organic synthesis, particularly in the preparation of various fluorinated compounds. It is also known for its potential applications in the pharmaceutical industry, as a building block for the synthesis of drug candidates. The compound is characterized by its unique structure, which includes a central pentane chain connecting two trifluoroacetamide groups, providing it with specific reactivity and properties that are valuable in chemical research and development.

2317-69-3

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2317-69-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2317-69-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,1 and 7 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2317-69:
(6*2)+(5*3)+(4*1)+(3*7)+(2*6)+(1*9)=73
73 % 10 = 3
So 2317-69-3 is a valid CAS Registry Number.

2317-69-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Di-trifluoracetyl-diaminopentan-(1,5)

1.2 Other means of identification

Product number -
Other names -

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:2317-69-3 SDS

2317-69-3Downstream Products

2317-69-3Relevant academic research and scientific papers

Systematic elucidation of crystal structure of fluorinated gemini-type diamide derivatives having different lengths with thixotropic induced-ability to solvents

Fujimori, Atsuhiro,Fukushi, Keito,Maruyama, Haruka,Okano, Rei,Satou, Eiichi,Yajima, Tomoko

, (2020)

Molecular packing structures for Gemini-type diamide derivatives with different linker and fluoroalkyl chain lengths were systematically determined using reciprocal lattice analysis. Diamide derivatives with two fluorocarbons, in which the linker was replaced with one hexamethylene chain and one pentamethylene chain, exhibited hydrogen bonding and crystallinity. Powder X-ray diffraction profiles displayed extremely sharp diffraction peaks like inorganic materials. Small-angle X-ray scattering analysis indicated extended chain crystals (ECCs) in these molecular groups. Reciprocal lattice analysis and high crystallinity allowed for the development of packing models for all compounds used in this study. Fifteen compounds were assigned to nearly orthorhombic and/or slightly distorted monoclinic systems, with one exception. All fluorinated Gemini-type diamides are characterized by a developed c-axis and have an ab-plane area that can accommodate a fluorocarbon chain. These fluorinated Gemini-type diamide derivatives are candidates for additive molecules to induce solvent thixotropy and form crystalline nanofibers through intermolecular hydrogen bonding. A correlation was found between molecular chain packing and crystal growth; a helical growth mode that permits gel formation by incorporating solvent molecules was also confirmed.

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