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N-Ethoxycarbonyl-3-nitro-p-toluidine, a yellow crystalline solid with the molecular formula C11H13N3O4 and a molecular weight of 243.24 g/mol, is a chemical compound that serves as an intermediate in the synthesis of pharmaceuticals and dyes. Classified as a nitro compound, it contains a nitro group, which endows it with reactivity and potential explosiveness if mishandled. Additionally, it is toxic if ingested or inhaled and can cause skin and eye irritation upon contact, necessitating careful handling and adherence to safety protocols in laboratory settings.

16648-53-6

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16648-53-6 Usage

Uses

Used in Pharmaceutical Industry:
N-Ethoxycarbonyl-3-nitro-p-toluidine is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its reactivity and unique chemical structure make it a valuable component in the development of new drugs and medications.
Used in Dye Industry:
In the dye industry, N-Ethoxycarbonyl-3-nitro-p-toluidine is utilized as an intermediate in the production of dyes. Its chemical properties contribute to the creation of a wide range of colorants used in various applications, such as textiles, plastics, and printing inks.

Check Digit Verification of cas no

The CAS Registry Mumber 16648-53-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,6,4 and 8 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 16648-53:
(7*1)+(6*6)+(5*6)+(4*4)+(3*8)+(2*5)+(1*3)=126
126 % 10 = 6
So 16648-53-6 is a valid CAS Registry Number.

16648-53-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl N-(4-methyl-3-nitrophenyl)carbamate

1.2 Other means of identification

Product number -
Other names ethyl 3-nitro-4-methylphenylcarbamate

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:16648-53-6 SDS

16648-53-6Relevant academic research and scientific papers

Design, synthesis, and anti-inflammatory properties of orally active 4-(phenylamino)-pyrrolo[2,1-f][1,2,4]triazine p38α mitogen-activated protein kinase inhibitors

Hynes Jr., John,Dyckman, Alaric J.,Lin, Shuqun,Wrobleski, Stephen T.,Wu, Hong,Gillooly, Kathleen M.,Kanner, Steven B.,Lonial, Herinder,Loo, Derek,McIntyre, Kim W.,Pitt, Sidney,Ding, Ren Shen,Shuster, David J.,Yang, XiaoXia,Zhang, Rosemary,Behnia, Kamelia,Zhang, Hongjian,Marathe, Punit H.,Doweyko, Arthur M.,Tokarski, John S.,Sack, John S.,Pokross, Matthew,Kiefer, Susan E.,Newitt, John A.,Barrish, Joel C.,Dodd, John,Schieven, Gary L.,Leftheris, Katerina

, p. 4 - 16 (2008/09/18)

A novel structural class of p38 mitogen-activated protein (MAP) kinase inhibitors consisting of substituted 4-(phenylamino)-pyrrolo[2,1-f][1,2,4] triazines has been discovered. An initial subdeck screen revealed that the oxindole-pyrrolo[2,1-f][1,2,4]tria

The Biodegradation of Low-molecular-weight Urethane Compounds by a Strain of Exophiala jeanselmei

Owen, Stephen,Otani, Takahito,Masaoka, Satoshi,Ohe, Tatsuhiko

, p. 244 - 248 (2007/10/03)

To further analyze the biodegradation of polyurethane polymers, we investigated the biodegradation of low-molecular-weight N-tolylcarbamate model compounds with structures closely resembling the urethane linkages found in polyurethanes based on tolylene-diisocyanate (TDT). Soil microflora were screened for microorganisms that were able to utilize toluene-2,4-dicarbamic acid, diethyl ester (compound 1) as the sole source of carbon, and the soil fungus Exophiala jeanselmei strain REN-11A was selected as the most effective strain. Several N-tolylcarbamate compounds were used, and it was found that REN-11A was able to degrade compound 1, as well as the related compound toluene-2,6-dicarbamic acid, diethyl ester, very efficiently. Further investigation showed that compound 1 was biodegraded to tolylene-2,4-diamine via the aromatic amine intermediates carbamic acid, (3-amino-4-methylphenyl)-, ethyl ester and carbamic acid, (5-amino-2-methylphenyl)-, ethyl ester.

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