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103796-12-9

4,N,N-trimethyl-3-nitrobenzenamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 103796-12-9 Structure

  • Basic information

    1. Product Name: 4,N,N-trimethyl-3-nitrobenzenamine
    2. Synonyms: 4,N,N-trimethyl-3-nitrobenzenamine
    3. CAS NO:103796-12-9
    4. Molecular Formula:
    5. Molecular Weight: 180.206
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 103796-12-9.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: 4,N,N-trimethyl-3-nitrobenzenamine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4,N,N-trimethyl-3-nitrobenzenamine(103796-12-9)
    11. EPA Substance Registry System: 4,N,N-trimethyl-3-nitrobenzenamine(103796-12-9)

  • 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: 103796-12-9(Hazardous Substances Data)

103796-12-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103796-12-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,7,9 and 6 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 103796-12:
(8*1)+(7*0)+(6*3)+(5*7)+(4*9)+(3*6)+(2*1)+(1*2)=119
119 % 10 = 9
So 103796-12-9 is a valid CAS Registry Number.

103796-12-9Relevant articles and documents

Mono-nitration of aromatic compounds via their nitric acid salts

Zhang, Pingsheng,Cedilote, Miall,Cleary, Thomas P.,Pierce, Michael E.

, p. 8659 - 8664 (2008/03/30)

Aromatic compounds bearing a basic nitrogen atom can be converted to the corresponding nitric acid salts. Mono-nitration of the compounds can be carried out by adding a dichloromethane solution of the salts to sulfuric acid, or by adding acetyl chloride (or trifluoroacetic anhydride) to a dichloromethane solution of the salts. This protocol provides, among other benefits, the most convenient and reliable way for the prevention of over-/under-nitration and is especially suitable for scale-up.

Mono-nitration of aromatic compounds via nitrate salts

-

Page/Page column 11-12, (2008/06/13)

A method of nitrating a compound selected from the group consisting of is provided.

ipso-Attack in the Nitration of Aromatic Amines. Part 3. Evidence for Two Mechanisms of ipso-Attack

Al-Omran, Fatima,Ridd, John H.

, p. 1185 - 1190 (2007/10/02)

Studies on the nitration of NN-dimethyl-4-methylaniline (1a) have been extended to NN-dimethyl-3,4-dimethylaniline (1b) and NN-dimethyl-3,4,5-trimethylaniline (1c).All three amines react with nitric acid in 60-70percent sulphuric acid at 0 deg C by the ni

ipso-Attack in the Nitration of Aromatic Amines. Part 1. The Reactions of NN-Dimethyl-p-toluidine and Some Related Compounds

Omran, Fatima Al-,Fujiwara, Kenji,Giffney, Janet C.,Ridd, John H.,Robinson, Stephen R.

, p. 518 - 525 (2007/10/02)

NN-Dimethyl-p-toluidine, NN-dimethyl-4-ethylaniline and NN-dimethyl-2,4,6-trimethylaniline react with nitric acid in aqueous sulphuric acid (ca. 70percent) to form the ipso-Wheland intermediates with an NO2 group at the 4-position (identified by (1)H and

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