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1,3,2-Dioxaphospholan-2-amine, 2,2-difluoro-2,2-dihydro-4,4,5,5-tetrakis(trifluoromethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

63173-83-1

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63173-83-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63173-83-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,1,7 and 3 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 63173-83:
(7*6)+(6*3)+(5*1)+(4*7)+(3*3)+(2*8)+(1*3)=121
121 % 10 = 1
So 63173-83-1 is a valid CAS Registry Number.

63173-83-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-difluoro-4,4,5,5-tetrakis(trifluoromethyl)-1,3,2λ5-dioxaphospholane-2-amine

1.2 Other means of identification

Product number -
Other names 2,2-difluoro-4,4,5,5-tetrakis-trifluoromethyl-2λ5-[1,3,2]dioxaphospholan-2-ylamine

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:63173-83-1 SDS

63173-83-1Upstream product

63173-83-1Downstream Products

63173-83-1Relevant academic research and scientific papers

Oxidative Additionen an 2-Amino-4,4,5,5-tetrakis(trifluormethyl)-1,3,2-dioxaphospholan

Storzer, Werner,Roeschenthaler, Gerd-Volker,Schmutzler, Reinhard,Sheldrick, William S.

, p. 3609 - 3624 (2007/10/02)

Oxidative addition of HF, Cl2, and (CF3)2CO to the title compound 6 furnishes the phosphoranes 2, 9, and 3, respectively.In the case of NH4 (4) the hydrospirophosphorane 1 is obtained via a substitution reaction followed by an oxidative addition.Compound 9 is a precursor for the aminotetraalkoxyphosphoranes 5, 8, and the very stable phosphazene 10 which is formed by loss of HCl by thermolysis.Due to a slow ligand exchange the 19F NMR spectrum of phosphorane 3 exhibits eight magnetically non equivalent CF3 groups.By means of 19F homodecoupling experiments extensive through space coupling is found in the molecule.The x-ray structure analysis of 3 shows a slight distortion from the trigonal bipyramidal geometry at phosphorus.For comparison, F2PNH2 and tBu2PNH2 react with (CF3)2CO to form (CF3)2C=NH, the aminofluorophosphorane 11, F2P(=O)OCH(CF3)2 (13), tBu2P(=O)H (12) and tBu2P(=O)OCH(CF3)2 (14), respectively.

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