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N-(2-BroMoethyl)urethane, also known as N-(2-bromomethyl)-N'-(2,2,2-trifluoroethyl)urea, is an organic compound with the molecular formula C5H8BrF3N2O. It is a pale yellow oil at room temperature and is characterized by its unique chemical structure, which includes a urea group and a bromomethyl group attached to different carbon atoms. N-(2-BroMoethyl)urethane is known for its reactivity and is commonly utilized in the synthesis of various chemical products.

7452-78-0

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7452-78-0 Usage

Uses

Used in Pest Control Industry:
N-(2-BroMoethyl)urethane is used as a key intermediate in the preparation of chiral carbamate butanoates, which are effective pest control agents. These chiral carbamates are designed to target specific pests, providing a more selective and environmentally friendly approach to pest management. N-(2-BroMoethyl)urethane's reactivity and unique structure enable the development of novel carbamate derivatives with improved biological activity and reduced environmental impact.

Check Digit Verification of cas no

The CAS Registry Mumber 7452-78-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,5 and 2 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7452-78:
(6*7)+(5*4)+(4*5)+(3*2)+(2*7)+(1*8)=110
110 % 10 = 0
So 7452-78-0 is a valid CAS Registry Number.
InChI:InChI=1/C5H10BrNO2/c1-2-9-5(8)7-4-3-6/h2-4H2,1H3,(H,7,8)

7452-78-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl N-(2-bromoethyl)carbamate

1.2 Other means of identification

Product number -
Other names (2-bromo-ethyl)-carbamic acid ethyl ester

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:7452-78-0 SDS

7452-78-0Relevant academic research and scientific papers

Synthesis of benzannulated N-heterocycles by a palladium-catalyzed C-C/C-N coupling of bromoalkylamines

Thansandote, Praew,Raemy, Manuel,Rudolph, Alena,Lautens, Mark

, p. 5255 - 5258 (2008/09/17)

(Chemical Equation Presented) A palladium-catalyzed domino intermolecular alkylation/intramolecular amination of functionalized aryl iodides represents a new strategy for the synthesis of benzannulated N-heterocycles, affording functionalized indolines an

5-Lipoxygenase inhibitors: Synthesis and structure-activity relationships of a series of 1-aryl-2H,4H-tetrahydro-1,2,4-triazin-3-ones

Bhatia, Pramila A.,Brooks, Clint D. W.,Basha, Anwer,Ratajczyk, James D.,Gunn, Bruce P.,Bouska, Jennifer B.,Lanni, Carmine,Young, Patrick R.,Bell, Randy L.,Carter, George W.

, p. 3938 - 3950 (2007/10/03)

Synthetic routes were developed to access a variety of novel 1-aryl- 2H,4H-tetrahydro-1,2,4-triazin-3-one analogs which were evaluated as 5- lipoxygenase (5-LO) inhibitors. The parent structure, 1-phenylperhydro- 1,2,4-triazin-3-one (4), was found to be a

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