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3026-99-1

N-O-Tolyl-diacetamide, also known as N-(4-Methylphenyl)-N'-(2-oxoethyl)ethane-1,2-diamine, is an organic compound with the chemical formula C11H15NO2. It is a white crystalline solid that is soluble in water and various organic solvents. N-O-TOLYL-DIACETAMIDE is primarily used as a chemical intermediate in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. N-O-Tolyl-diacetamide is known for its reactivity and can be used in various chemical reactions, such as condensation and substitution, to form a wide range of products. Its structure consists of a tolyl group (a methyl-substituted phenyl group) attached to a diacetamide moiety, which contributes to its unique chemical properties and applications.

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  • 3026-99-1 Structure

  • Basic information

    1. Product Name: N-O-TOLYL-DIACETAMIDE
    2. Synonyms: N-O-TOLYL-DIACETAMIDE
    3. CAS NO:3026-99-1
    4. Molecular Formula: C11H13NO2
    5. Molecular Weight: 191.22642
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 3026-99-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 105-105.5 °C(Press: 1.2 Torr)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.118±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 0.29±0.50(Predicted)
    10. CAS DataBase Reference: N-O-TOLYL-DIACETAMIDE(CAS DataBase Reference)
    11. NIST Chemistry Reference: N-O-TOLYL-DIACETAMIDE(3026-99-1)
    12. EPA Substance Registry System: N-O-TOLYL-DIACETAMIDE(3026-99-1)

  • 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: 3026-99-1(Hazardous Substances Data)

3026-99-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3026-99-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,2 and 6 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3026-99:
(6*3)+(5*0)+(4*2)+(3*6)+(2*9)+(1*9)=71
71 % 10 = 1
So 3026-99-1 is a valid CAS Registry Number.

3026-99-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-acetyl-N-(2-methylphenyl)acetamide

1.2 Other means of identification

Product number -
Other names N-o-tolyl-diacetamide

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:3026-99-1 SDS

3026-99-1Relevant articles and documents

2-(Trifluoromethyl)indoles via Pd(0)-Catalyzed C(sp3)-H Functionalization of Trifluoroacetimidoyl Chlorides

Pedroni, Julia,Cramer, Nicolai

, p. 1932 - 1935 (2016/06/09)

Perfluoroalkylated indoles are valuable compounds in drug discovery. A Pd(0)-catalyzed C(sp3)-H functionalization enables access to 2-(trifluoromethyl)indoles from trifluoroacetimidoyl chlorides. These are stable compounds, easily obtained from

The ortho-substituted N,N-diacetylaniline as a selective acetylating reagent

Murakami, Yasuoki,Kondo, Kazuhiro,Miki, Kazuki,Akiyama, Yoko,Watanabe, Toshiko,Yokoyama, Yuusaku

, p. 3751 - 3754 (2007/10/03)

Selective acetylation of the less hindered amino group in the presence of the more hindered amino group with the use of 2-trifluoromethyl-N,N-diacetylaniline 2c is described. This acetylation with 2c yielded the corresponding less hindered monoacetamide exclusively, simply, conveniently, and in good yields.

Effect of substituents in the formation of diacetanilides

Ayyangar, Nagaraj R.,Srinivasan, Kumar V.

, p. 1292 - 1296 (2007/10/02)

A number of diacetanilides, including some which have not been reported so far, have been synthesized from the corresponding monoacetyl derivatives and characterized by spectral and elemental analyses.A tlc/fid method for the quantitative estimation of the relative amounts of mono- and diacetyl derivatives has been standardized.Linear correlation of the extent of diacetylation with Hammett ?-values of substituents and basicity constants of monoacetyl derivatives has been established.A plausible mechanism for the diacetylation reaction based on experimental observations has been suggested.An explanation for the anomalous behaviour of acetanilides containing electron-withdrawing substituents in the ortho-position has been put forth.

Aromatic Diazonium Salts, X. - A One-Pot Procedure for the Jacobson Synthesis of Indazole

Ruechardt, Christoph,Hassmann, Volker

, p. 908 - 927 (2007/10/02)

Procedures are described for a one-pot synthesis of 1H-indazole and substituted indazoles 3 in good yield (Table 1) from o-toluidines 2, alkyl nitrite or nitrous oxides, potassium acetate, and acetic anhydride in benzene.The spectroscopic properties of substituted indazoles (Tables 2-4) are discussed. - 4-Phenylcinnoline (18) is prepared by the same procedure from o-(α-methylenebenzyl)aniline.

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