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N-Ethoxycarbonyl-5-nitro-O-toluidine, a chemical compound with the molecular formula C11H12N2O4, is a yellow to orange crystalline powder. It is a nitroaromatic compound known for its potential toxic and mutagenic properties, necessitating careful handling and adherence to safety procedures.

16648-52-5

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16648-52-5 Usage

Uses

Used in Dye and Pigment Production:
N-Ethoxycarbonyl-5-nitro-O-toluidine is used as a key component in the production of dyes and pigments, contributing to the vibrant coloration of various products.
Used as a Chemical Intermediate in Pharmaceutical Synthesis:
N-ETHOXYCARBONYL-5-NITRO-O-TOLUIDINE serves as an intermediate in the synthesis of pharmaceuticals, playing a crucial role in the development of new medications.
Used as a Chemical Intermediate in Agrochemical Synthesis:
N-Ethoxycarbonyl-5-nitro-O-toluidine is also utilized as an intermediate in the creation of agrochemicals, which are essential for enhancing crop protection and yield.

Check Digit Verification of cas no

The CAS Registry Mumber 16648-52-5 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 2 respectively.
Calculate Digit Verification of CAS Registry Number 16648-52:
(7*1)+(6*6)+(5*6)+(4*4)+(3*8)+(2*5)+(1*2)=125
125 % 10 = 5
So 16648-52-5 is a valid CAS Registry Number.

16648-52-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl N-(2-methyl-5-nitrophenyl)carbamate

1.2 Other means of identification

Product number -
Other names Ethyl 2-methyl-5-nitrophenylcarbamate

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:16648-52-5 SDS

16648-52-5Relevant academic research and scientific papers

Installation of protected ammonia equivalents onto aromatic & heteroaromatic rings in water enabled by micellar catalysis

Isley, Nicholas A.,Dobarco, Sebastian,Lipshutz, Bruce H.

supporting information, p. 1480 - 1488 (2014/03/21)

A single set of conditions consisting of a palladium catalyst, a commercially available ligand, and a base, allow for several types of C-N bond constructions to be conducted in water with the aid of a commercially available "designer" surfactant (TPGS-750-M). Products containing a protected NH2 group in the form of a carbamate, sulfonamide, or urea can be fashioned starting with aryl or heteroaryl bromides, iodides, and in some cases, chlorides, as substrates. Reaction temperatures are in the range of room temperature to, at most, 50 °C, and result in essentially full conversion and good isolated yields.

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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