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53844-02-3

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53844-02-3 Usage

General Description

Benzyl 2-Bromoethylcarbamate is a chemical compound with a molecular formula of C11H12BrNO2. BENZYL 2-BROMOETHYLCARBAMATE belongs to the carbamate esters category, a type of salts or esters of carbamic acid. The carbamate group comprises both an amine and a carbonyl functional group. Generally, carbamates are used in organizing industrial products like pharmaceuticals, biocides, and plasticizers. Nonetheless, data regarding specific properties, uses, or potential health effects of Benzyl 2-Bromoethylcarbamate is somewhat limited, indicating it may not be widely utilized or studied.

Check Digit Verification of cas no

The CAS Registry Mumber 53844-02-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,8,4 and 4 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 53844-02:
(7*5)+(6*3)+(5*8)+(4*4)+(3*4)+(2*0)+(1*2)=123
123 % 10 = 3
So 53844-02-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H12BrNO2/c11-6-7-12-10(13)14-8-9-4-2-1-3-5-9/h1-5H,6-8H2,(H,12,13)

53844-02-3SDS

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 Benzyl (2-bromoethyl)carbamate

1.2 Other means of identification

Product number -
Other names N-Cbz-2-bromoethylamine

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:53844-02-3 SDS

53844-02-3Relevant articles and documents

Chemoselective and Highly Sensitive Quantification of Gut Microbiome and Human Metabolites

Conway, Louis P.,Globisch, Daniel,L?hr, J.-Matthias,Lin, Weifeng,Vujasinovic, Miroslav

, p. 23232 - 23240 (2021)

The microbiome has a fundamental impact on the human host's physiology through the production of highly reactive compounds that can lead to disease development. One class of such compounds are carbonyl-containing metabolites, which are involved in diverse biochemical processes. Mass spectrometry is the method of choice for analysis of metabolites but carbonyls are analytically challenging. Herein, we have developed a new chemical biology tool using chemoselective modification to overcome analytical limitations. Two isotopic probes allow for the simultaneous and semi-quantitative analysis at the femtomole level as well as qualitative analysis at attomole quantities that allows for detection of more than 200 metabolites in human fecal, urine and plasma samples. This comprehensive mass spectrometric analysis enhances the scope of metabolomics-driven biomarker discovery. We anticipate that our chemical biology tool will be of general use in metabolomics analysis to obtain a better understanding of microbial interactions with the human host and disease development.

N-bromosuccinimide promoted synthesis of β-amino bromides under Appel reaction condition

Chinthaginjala, Srinivasulu,Alavandimat, Nanda H.,Umesha, Vathsala,Sureshbabu, Vommina V.

supporting information, p. 2975 - 2983 (2021/08/27)

An efficient and facile method has been developed for the synthesis of chiral β-amino bromides from their corresponding alcohols under Appel reaction conditions. This approach allows for the deoxybromination of a variety of β-amino alcohols in excellent y

Method for catalyzing aldol self-condensation reaction of low-carbon aldehyde by acid alkali double-function ionic liquid

-

Paragraph 0050-0052, (2018/03/01)

The invention relates to a method for catalyzing aldol self-condensation reaction of low-carbon aldehyde by acid alkali double-function ionic liquid. The method comprises the following steps: adding low-carbon aldehyde and an acid alkali double-function ionic liquid catalyst into a high-pressure kettle, reacting at 60 to 150 DEG C for 1 to 12 hours, and performing hydroxyaldehyde self-condensationreaction on the low-carbon aldehyde to obtain long-chain unsaturated aldehyde, wherein the acid alkali double-function ionic liquid is the acid alkali double-function ionic liquid with cation and anion containing acid and alkali groups correspondingly, or the novel acid alkali double-function ionic liquid with cation containing acid and alkali groups. The method is applied to aldol self-condensation reaction of n-butanal and n-pentanal and is mild in reaction condition, high in catalytic activity and high in selectivity; and the acid alkali double-function ionic liquid catalyst can be reused.

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