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CAS

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92836-02-7

N-Methyl-N'-(4-methyl-3-nitro-phenyl)-benzamidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 92836-02-7 Structure

  • Basic information

    1. Product Name: N-Methyl-N'-(4-methyl-3-nitro-phenyl)-benzamidine
    2. Synonyms: N-Methyl-N'-(4-methyl-3-nitro-phenyl)-benzamidine
    3. CAS NO:92836-02-7
    4. Molecular Formula:
    5. Molecular Weight: 269.303
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 92836-02-7.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: N-Methyl-N'-(4-methyl-3-nitro-phenyl)-benzamidine(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-Methyl-N'-(4-methyl-3-nitro-phenyl)-benzamidine(92836-02-7)
    11. EPA Substance Registry System: N-Methyl-N'-(4-methyl-3-nitro-phenyl)-benzamidine(92836-02-7)

  • 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: 92836-02-7(Hazardous Substances Data)

92836-02-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92836-02-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,8,3 and 6 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 92836-02:
(7*9)+(6*2)+(5*8)+(4*3)+(3*6)+(2*0)+(1*2)=147
147 % 10 = 7
So 92836-02-7 is a valid CAS Registry Number.

92836-02-7Downstream Products

92836-02-7Relevant articles and documents

REACTIONS OF IMIDIC ACID DERIVATIVES WITH NUCLEOPHILIC REAGENTS. KINETICS OF THE REACTION OF N-SUBSTITUTED BENZIMIDOYL CHLORIDES WITH ARYLAMIDES IN APROTIC MEDIA. THE EFFECT OF THE STRUCTURE OF THE AMINE

Litvinenko, L. M.,Mikhailov, V. A.,Drizhd, L. P.,Savelova, V. A.,Kryuchkova, E. N.

, p. 1139 - 1143 (2007/10/02)

The kinetics of the reaction of primary aromatic amines H2NC6H4X with N-substituted benzimidoyl chlorides C6H5C(Cl)=NR in acetonitrile (R = CH3; COC6H5, SO2C6H5) and dioxane (R = CH3) at 25 grad C were studied.The sensitivity of the rate of the processes to variation in the substituent X in the arylamine depends substantially on the electronic nature of the substituent R in the in the imidoyl chloride, but isoparametric effects are not observed.It is supposed that this is due to the realization of a mechanism of bimolecular nucleophilic substitution at the imidoyl carbon atom through various transition states, depending on the substituent R at C=N bond.

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