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160754-06-3

3,4-dimethyl-2,6-dinitroanisole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 160754-06-3 Structure

  • Basic information

    1. Product Name: 3,4-dimethyl-2,6-dinitroanisole
    2. Synonyms: 3,4-dimethyl-2,6-dinitroanisole
    3. CAS NO:160754-06-3
    4. Molecular Formula:
    5. Molecular Weight: 226.189
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 160754-06-3.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: 3,4-dimethyl-2,6-dinitroanisole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,4-dimethyl-2,6-dinitroanisole(160754-06-3)
    11. EPA Substance Registry System: 3,4-dimethyl-2,6-dinitroanisole(160754-06-3)

  • 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: 160754-06-3(Hazardous Substances Data)

160754-06-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 160754-06-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,7,5 and 4 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 160754-06:
(8*1)+(7*6)+(6*0)+(5*7)+(4*5)+(3*4)+(2*0)+(1*6)=123
123 % 10 = 3
So 160754-06-3 is a valid CAS Registry Number.

160754-06-3Downstream Products

160754-06-3Relevant articles and documents

Process and intermediate to prepare N-alkyl-3,4-dialkyl-2,6-dinitro-anilines

-

, (2008/06/13)

The intermediate STR1 wherein R is a lower alkyl group, is used to prepare a N-alkyl-3,4-dialkyl-2,6,-dinitro-aniline in a relatively simple, inexpensive and safe fashion, and with a high yield.

Novel process to prepare N-alkyl-3,4-dialkyl-2,6-dinitroanilines

-

, (2008/06/13)

A process is provided for preparing N-alkyl-3,4-dialkyl-2,6-dinitroanilines of the formula Wherein R1 is hydrogen, C1 to C6 straight or branched chain alkyl group; and, R2, R3 and R4 are independently C1 to C6 straight or branched chain alkyl group optionally substituted by one or more halogen groups, wherein a. 3,4-dialkyl phenol of the formula is selectively nitrated with nitric acid in a two phase system to form 3,4-dialkyl-2,6-dinitrophenol of the formula: b. the 3,4-dialkyl-2,6-dinitrophenol is alkylated with an alkylating agent in the presence of a base and a catalytic amount of a phase transfer catalyst chosen from the group consisting of, , (R')4Q X-, , wherein R' may be the same or different C1 to C16 straight or branched alkyl groups, benzyl, substituted benzyl; Qis N or P; and Xis CL, Br, I or HSO4; a macrocyclic ether and polyethylene glycols of formula, , HO - (CH2CH2O-)n-CH2CH2OH, , where n is an integer from 10 to 50, in an organic solvent to form 3,4-dalkyl-2,6-dinitro alkoxybenzene of the formula: where R5 is an alkyl group having 1 to 6 carbon atoms. c. the 3,4-dialkyl-2,6-dinitro alkoxybenzene is reacted with an amine of the formula where R1 and R2 are defined above, in the presence of a catalytic amount of base or halide to form N-alkyl-3,4-dialkyl-2,6-dinitroaniline. d. the N-alkyl-3,4-dialkyl-2,6-dinitroaniline is recovered.

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