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N1-isobutyl-4-(trifluoromethyl)benzene-1,2-diamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 908369-02-8 Structure
  • Basic information

    1. Product Name: N1-isobutyl-4-(trifluoromethyl)benzene-1,2-diamine
    2. Synonyms: N1-isobutyl-4-(trifluoromethyl)benzene-1,2-diamine
    3. CAS NO:908369-02-8
    4. Molecular Formula:
    5. Molecular Weight: 232.249
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 908369-02-8.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: N1-isobutyl-4-(trifluoromethyl)benzene-1,2-diamine(CAS DataBase Reference)
    10. NIST Chemistry Reference: N1-isobutyl-4-(trifluoromethyl)benzene-1,2-diamine(908369-02-8)
    11. EPA Substance Registry System: N1-isobutyl-4-(trifluoromethyl)benzene-1,2-diamine(908369-02-8)
  • 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: 908369-02-8(Hazardous Substances Data)

908369-02-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 908369-02-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,8,3,6 and 9 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 908369-02:
(8*9)+(7*0)+(6*8)+(5*3)+(4*6)+(3*9)+(2*0)+(1*2)=188
188 % 10 = 8
So 908369-02-8 is a valid CAS Registry Number.

908369-02-8Relevant articles and documents

A Novel Mechanistic Study on Ultrasound-Assisted, One-Pot Synthesis of Functionalized Benzimidazo[2,1-b]quinazolin-1(1H)-ones

Chen, Li-Hsun,Chung, Tsai-Wen,Narhe, Bharat D.,Sun, Chung-Ming

, p. 162 - 169 (2016)

Ultrasound-assisted synthesis of benzimidazo[2,1-b]quinazolin-1(1H)-ones was achieved via piperidine-catalyzed three-component reaction of 2-aminobenzimidazoles, an aromatic aldehyde, and 1,3-dione in aqueous isopropanol. This mechanism was first suspected following our identification of unusual reaction intermediates in a one-pot reaction. An unprecedented coupling reaction, it involved a nucleophilic attack by 2-aminobenzimidazole on in situ generated Michael adduct, followed by electrocyclic ring formation reaction. In contrast to the commonly accepted mechanism, that the direct reaction of 2-amino benzimidazole with a Knoevenagel adduct cannot deliver target compounds.

FUSED HETEROCYCLIC COMPOUND AND USE THEREOF

-

Page/Page column 244, (2010/11/17)

A fused heterocyclic compound of formula (1): wherein, A1 and A2 represent a nitrogen atom or the like, R1, R2, R3 and R4 represent a halogen atom or the like, R2 and R3 represent a halogen atom or the like, R5 represents a C1-C6 chain hydrocarbon group optionally substituted with one or more halogen atoms, or the like, R6 and R7 represent a C1-C4 chain hydrocarbon group substituted with one or more halogen atoms, or the like, and n represents 0 or 1, has an excellent noxious arthropod controlling effect.

Flavin-based [2]rotaxanes

Cooke, Graeme,Garety, James F.,Jordan, Brian,Kryvokhyzha, Nadiya,Parkin, Andy,Rabani, Gouher,Rotello, Vincent M.

, p. 2297 - 2300 (2007/10/03)

We report the synthesis of flavin-stoppered hydrogen bonded [2]rotaxanes 1 and 2. We also report the electrochemically controllable properties of these systems in solution, and for derivative 2, as an electropolymerized thin film.

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