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105891-08-5

Benzenemethanamine, N-(diphenylmethylene)-a-isocyanato-a-(trifluoromethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 105891-08-5 Structure

  • Basic information

    1. Product Name: Benzenemethanamine, N-(diphenylmethylene)-a-isocyanato-a-(trifluoromethyl)-
    2. Synonyms:
    3. CAS NO:105891-08-5
    4. Molecular Formula: C22H15F3N2O
    5. Molecular Weight: 380.369
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 105891-08-5.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: Benzenemethanamine, N-(diphenylmethylene)-a-isocyanato-a-(trifluoromethyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzenemethanamine, N-(diphenylmethylene)-a-isocyanato-a-(trifluoromethyl)-(105891-08-5)
    11. EPA Substance Registry System: Benzenemethanamine, N-(diphenylmethylene)-a-isocyanato-a-(trifluoromethyl)-(105891-08-5)

  • 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: 105891-08-5(Hazardous Substances Data)

105891-08-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105891-08-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,8,9 and 1 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 105891-08:
(8*1)+(7*0)+(6*5)+(5*8)+(4*9)+(3*1)+(2*0)+(1*8)=125
125 % 10 = 5
So 105891-08-5 is a valid CAS Registry Number.

105891-08-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(1-phenyl-1-isocyanato-2,2,2-trifluoroethyl)diphenylketimine

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:105891-08-5 SDS

105891-08-5Downstream Products

105891-08-5Relevant articles and documents

N-CARBODIIMIDES. ISOMERIC TRANSFORMATIONS AND REACTIONS WITH PROTON-CONTAINING NUCLEOPHILIC REAGENTS

Vovk, M. V.,Dorokhov, V. I.,Samarai, L. I.

, p. 654 - 658 (2007/10/02)

The conditions for the isomerization of N-carbodiimides to N-alkylidene-N'-acylureas were investigated.In the reaction of N-carbodiimides with alcohols, phenols, thiophenols, and imines fragmentation of the carbodiimides occurs with the formation of 1-alkoxy-, 1-aryloxy-, 1-arylthio-, and 1-alkylideneaminoalkyl isocyanates and amides.The products from the reaction with water and with tert-butylamine are the amide, ketone, and N-alkylimine.

THERMAL REARRANGEMENT OF DIALKYLIDENEUREAS INTO α-(ALKYLIDENEAMINO)ALKYL ISOCYANATES

Gorbatenko, V. I.,Mel'nichenko, N. V.,Samarai, L. I.

, p. 1064 - 1068 (2007/10/02)

The thermal rearrangement of bisalkylideneureas to α-(alkylideneamino)alkyl isocyanates was studied.Its limits and the relationships governing it were determined.The mechanism of rearrangement is discussed on the basis of the kinetic measurements.

PSEUDOHALOGEN CHARACTER OF THE HETEROCUMULENE GROUP IN GEM-DI(HETEROCUMULENO)ALKANES

Gorbatenko, V. I.,Mel'nichenko, N. V.,Samarai, L. I.

, p. 2020 - 2023 (2007/10/02)

In the reactions of gem-di(heterocumuleno)alkanes with triphenylphosphoranediylaminotrimethylsilane or N-(trimethylsilyl)diphenylketimine one heterocumulene group (isocyanate or carbodiimide) exhibits pseudohalogen characteristics.A new rearrangement with migration of the N=C(C6H5)2 group was discovered in the azaallyl triad C=N-C.

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