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2-<3,3-dimethyl-5,5-bis(trifluoromethyl)-1-pyrazolin-1-ylio>-1,1,1-trifluoro-2-azaethan-2-ide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 85122-33-4 Structure
  • Basic information

    1. Product Name: 2-<3,3-dimethyl-5,5-bis(trifluoromethyl)-1-pyrazolin-1-ylio>-1,1,1-trifluoro-2-azaethan-2-ide
    2. Synonyms: 2-<3,3-dimethyl-5,5-bis(trifluoromethyl)-1-pyrazolin-1-ylio>-1,1,1-trifluoro-2-azaethan-2-ide
    3. CAS NO:85122-33-4
    4. Molecular Formula:
    5. Molecular Weight: 317.157
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 85122-33-4.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-<3,3-dimethyl-5,5-bis(trifluoromethyl)-1-pyrazolin-1-ylio>-1,1,1-trifluoro-2-azaethan-2-ide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-<3,3-dimethyl-5,5-bis(trifluoromethyl)-1-pyrazolin-1-ylio>-1,1,1-trifluoro-2-azaethan-2-ide(85122-33-4)
    11. EPA Substance Registry System: 2-<3,3-dimethyl-5,5-bis(trifluoromethyl)-1-pyrazolin-1-ylio>-1,1,1-trifluoro-2-azaethan-2-ide(85122-33-4)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 85122-33-4(Hazardous Substances Data)

85122-33-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85122-33-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,1,2 and 2 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 85122-33:
(7*8)+(6*5)+(5*1)+(4*2)+(3*2)+(2*3)+(1*3)=114
114 % 10 = 4
So 85122-33-4 is a valid CAS Registry Number.

85122-33-4SDS

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 2-[3,3-dimethyl-5,5-bis(trifluoromethyl)-1-pyrazolin-1-ylio]-1,1,1-trifluoro-2-azaethan-2-ide

1.2 Other means of identification

Product number -
Other names 2-(3,3-dimethyl-5,5-bis(trifluoromethyl)-1-pyrazolin-1-ylio)-1,1,1-trifluoro-2-azaethan-2-ide

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:85122-33-4 SDS

85122-33-4Relevant articles and documents

Unsaturated nitrogen compounds containing fluorine. Part 13. Reaction of 2--1,1,1,3,3,3-hexafluoropropan-2-ide with compounds containing N=O or N-O bonds

Bell, David,Tipping, Anthony E.

, p. 279 - 286 (1994)

Reaction of the title azomethinimine (1) with nitrogen dioxide gives nitric oxide, hexafluoroacetone and 3,3-dimethyl-5,5-bis(trifluoromethyl)-1-pyrazoline (2) in high yield, while with the perfluoronitrosoalkanes RFNO (RF = CF3 and CF2CF2CF3) the products are hexafluoroacetone and the azimines 8a and 8b, respectively.The reactions involve initial cycloaddition involving the N=O bonds, followed by elimination of hexafluoroacetone and niric oxide to give 2 or of hexafluoroacetone to give 8.From reaction of 1 with nitrosyl chloride the major products are nitric oxide, 7-chloro-8,8,8-trifluoro-2-methyl-4,4,7-tris(trifluoromethyl) -5,6-diazaocta-1,5-diene (13) and 5,5-dimethyl-3,3-bis(trifluoromethyl)-1-pyrazolidine (14) formed via decomposition of the 1:1 adduct containing C-chloro and N-nitroso substituents.The oxyl (CF3)2NO. attacks azomethinimine 1 at carbon and the resulting 1:1 adduct decomposes to give hexafluoroacetone, the pyrazoline 2 and (CF3)2N. radicals which are trapped by the oxyl to afford the oxadiazapentane (CF3)2NON(CF3)2 (19).Secondary reaction then takes place involving attack of the oxygen atom of the oxadiazapentane on 1 at carbon to give hexafluoroacetone, N,N-bis(trifluoromethyl)amine and 3-methyl-5,5-bis(trifluoromethyl)-3--1-pyrazoline (21).This is confirmed by treatment of 1 with the oxadiazapentane 19.

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