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2354-93-0

Carbamic acid, [3-(trifluoromethyl)phenyl]-, ethyl ester (9CI) is an organic compound with the chemical formula C10H10F3NO2. It is a derivative of carbamic acid, featuring a trifluoromethylphenyl group at the 3-position and an ethyl ester group. Carbamic acid,[3-(trifluoromethyl)phenyl]-, ethyl ester (9CI) is characterized by its molecular weight of 239.19 g/mol and a melting point of 40-42°C. It is a colorless to pale yellow liquid and is soluble in organic solvents. The compound is primarily used as an intermediate in the synthesis of various agrochemicals, pharmaceuticals, and other chemical products. Due to its potential applications in these fields, it is important to understand its chemical properties and reactivity.

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  • 2354-93-0 Structure

  • Basic information

    1. Product Name: Carbamic acid,[3-(trifluoromethyl)phenyl]-, ethyl ester (9CI)
    2. Synonyms: Carbanilicacid, m-(trifluoromethyl)-, ethyl ester (7CI,8CI); NSC 51605
    3. CAS NO:2354-93-0
    4. Molecular Formula: C10H10 F3 N O2
    5. Molecular Weight: 233.19
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 2354-93-0.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: Carbamic acid,[3-(trifluoromethyl)phenyl]-, ethyl ester (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Carbamic acid,[3-(trifluoromethyl)phenyl]-, ethyl ester (9CI)(2354-93-0)
    11. EPA Substance Registry System: Carbamic acid,[3-(trifluoromethyl)phenyl]-, ethyl ester (9CI)(2354-93-0)

  • 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: 2354-93-0(Hazardous Substances Data)

2354-93-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2354-93-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,5 and 4 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2354-93:
(6*2)+(5*3)+(4*5)+(3*4)+(2*9)+(1*3)=80
80 % 10 = 0
So 2354-93-0 is a valid CAS Registry Number.

2354-93-0SDS

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-[3-(trifluoromethyl)phenyl]carbamate

1.2 Other means of identification

Product number -
Other names N-<3-Trifluormethyl-phenyl>-carbamidsaeureaethylester

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:2354-93-0 SDS

2354-93-0Relevant articles and documents

An efficient one-pot synthesis of: N, N ′-disubstituted ureas and carbamates from N -acylbenzotriazoles

Singh, Anoop S.,Kumar, Dhananjay,Mishra, Nidhi,Tiwari, Vinod K.

, p. 84512 - 84522 (2016/10/12)

A facile and high-yielding one-pot synthesis of carbamates and N,N′-disubstituted symmetrical ureas from N-acylbenzotriazoles has been devised. It is believed that, the intermediate acyl-azide undergo Curtius rearrangement and in different solvents gives different products i.e. carbamates in alcohols and N,N′-disubstituted symmetrical urea in THF.

1,7-palladium migration via C-H activation, followed by intramolecular amination: Regioselective synthesis of benzotriazoles

Zhou, Jun,He, Jianjun,Wang, Binjie,Yang, Weijun,Ren, Hongjun

supporting information; experimental part, p. 6868 - 6870 (2011/06/21)

A novel 1,7-palladiummigration-cyclization-dealkylation sequence for the regioselective synthesis of benzotriazoles has been developed. These reactions proceed in excellent yields with high regioselectivities. The mechanism of the reaction has also been investigated.

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