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N-(2,3-DiMethyl-6-nitrophenyl)acetaMide is a chemical compound characterized by its molecular formula C10H12N2O3. It is a yellow crystalline powder that serves as an intermediate in the synthesis of pharmaceuticals and agrochemicals. N-(2,3-DiMethyl-6-nitrophenyl)acetaMide is distinguished by its nitro group, a methyl group, and an amide functional group, which contribute to its versatility in chemical reactions and applications. Its potential use as a building block in the development of new drugs and pesticides is notable, given the presence of the nitro group. Careful handling and adherence to safety protocols are essential when working with this chemical.

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  • 138330-47-9 Structure
  • Basic information

    1. Product Name: N-(2,3-DiMethyl-6-nitrophenyl)acetaMide
    2. Synonyms: N-(2,3-DiMethyl-6-nitrophenyl)acetaMide;2',3'-Dimethyl-6'-nitroacetanilide
    3. CAS NO:138330-47-9
    4. Molecular Formula: C10H12N2O3
    5. Molecular Weight: 208.21388
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 138330-47-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: N-(2,3-DiMethyl-6-nitrophenyl)acetaMide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(2,3-DiMethyl-6-nitrophenyl)acetaMide(138330-47-9)
    11. EPA Substance Registry System: N-(2,3-DiMethyl-6-nitrophenyl)acetaMide(138330-47-9)
  • 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: 138330-47-9(Hazardous Substances Data)

138330-47-9 Usage

Uses

Used in Pharmaceutical Industry:
N-(2,3-DiMethyl-6-nitrophenyl)acetaMide is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its presence of a nitro group and amide functional group makes it a valuable component in the development of new drugs, potentially enhancing their therapeutic properties and effectiveness.
Used in Agrochemical Industry:
In the agrochemical sector, N-(2,3-DiMethyl-6-nitrophenyl)acetaMide is utilized as an intermediate in the production of pesticides. Its chemical structure, including the nitro group, allows for the creation of compounds that can effectively control and manage pests, thereby contributing to improved crop protection and yield.
Used in Chemical Research:
N-(2,3-DiMethyl-6-nitrophenyl)acetaMide is also employed in chemical research as a versatile compound for conducting various chemical reactions. Its unique structure facilitates the exploration of new reaction pathways and the synthesis of novel compounds with potential applications in different fields.

Check Digit Verification of cas no

The CAS Registry Mumber 138330-47-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,3,3 and 0 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 138330-47:
(8*1)+(7*3)+(6*8)+(5*3)+(4*3)+(3*0)+(2*4)+(1*7)=119
119 % 10 = 9
So 138330-47-9 is a valid CAS Registry Number.
InChI:InChI=1S/C10H12N2O3/c1-6-4-5-9(12(14)15)10(7(6)2)11-8(3)13/h4-5H,1-3H3,(H,11,13)

138330-47-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2,3-Dimethyl-6-nitrophenyl)acetamide

1.2 Other means of identification

Product number -
Other names 2',3'-DIMETHYL-6'-NITROACETANILIDE

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:138330-47-9 SDS

138330-47-9Relevant articles and documents

Detection and Imaging of Nitric Oxide with Novel Fluorescent Indicators: Diaminofluoresceins

Kojima, Hirotatsu,Nakatsubo, Naoki,Kikuchi, Kazuya,Kawahara, Shigenori,Kirino, Yutaka,Nagoshi, Hiroshi,Hirata, Yasunobu,Nagano, Tetsuo

, p. 2446 - 2453 (1998)

Nitric oxide is a gaseous, free radical which plays a role as an intracellular second messenger and a diffusable intercellular messenger. To obtain direct evidence for NO functions in vivo, we have designed and synthesized diaminofluoresceins (DAFs) as no

Diaminofluorescein derivative

-

, (2008/06/13)

A compound represented by the following formula (I): wherein R1and R2represent amino group that substitute at adjacent positions on the phenyl ring, provided that either of R1and R2represents a mono(C1-6/s

Substituted 2-arylimino heterocycles and compositions containing them, for use as progesterone receptor binding agents

-

Page column 152, (2010/02/05)

This invention relates to 2-arylimino heterocycles, including 2-arylimino-1,3-thiazolidines, 2-arylimino-2,3,4,5-tetrahydro-1,3-thiazines, 2-arylimino-1,3-thiazolidin-4-ones, 2-arylimino-1,3-thiazolidin-5-ones, and 2-arylimino-1,3-oxazolidines, and their use in modulating progesterone receptor mediated processes, and pharmaceutical compositions for use in such therapies.

Ozone-mediated Reaction of Anilides and Phenyl Esters with Nitrogen Dioxide: Enhanced Ortho-reactivity and Mechanistic Implications

Suzuki, Hitomi,Tatsumi, Atsuo,Ishibashi, Taro,Mori, Tadashi

, p. 339 - 344 (2007/10/02)

In the presence of ozone, anilides 1 can be nitrated rapidly with nitrogen dioxide in chloroform at 0 deg C to give a high proportion of ortho-nitro derivatives (ortho:para = 1.2-4.4) in good yields.The phenyl esters 15 can be similarly nitrated on the aromatic ring without significant cleavage of the ester bond, giving a mixture of isomeric nitro derivatives in which the ortho-isomer predominantes (ortho:para = 1.1-1.5).The oridin of the enhanced ortho reactivity is discussed in terms of an electron-transfer process involving the nitrogen trioxide as initial electrophile.

Ortho-Selective Nitration of Acetanilides with Nitrogen Dioxide in the Presence of Ozone

Suzuki, Hitomi,Ishibashi, Taro,Murashima, Takashi,Tsukamoto, Kenkichi

, p. 6591 - 6594 (2007/10/02)

In the presence of ozone, nitrogen dioxide rapidly reacts with acetanilides ortho-selectively at low temperatures, giving a high proportion of ortho-nitro derivatives in good yields.

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