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29823-21-0

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  • 29823-21-0 Structure

  • Basic information

    1. Product Name: 8-BROMOOCTANOIC ACID ETHYL ESTER
    2. Synonyms: ETHYL W-BROMOOCTANOATE;ETHYL 8-BROMOOCTANOATE;ETHYL OMEGA-BROMOOCTANOATE;8-BROMOOCTANOIC ACID ETHYL ESTER;8-CAPRYLIC ACID ETHYL ESTER;8-Bromooctanoic Ethylester;Ethyl 8-bromoocatanoate;Nsc100182
    3. CAS NO:29823-21-0
    4. Molecular Formula: C10H19BrO2
    5. Molecular Weight: 251.16
    6. EINECS: 1312995-182-4
    7. Product Categories: N/A
    8. Mol File: 29823-21-0.mol
    9. Article Data: 1

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 123°C/ 3mm
    3. Flash Point: 139.5 °C
    4. Appearance: /
    5. Density: 1.194
    6. Vapor Pressure: 0.00831mmHg at 25°C
    7. Refractive Index: 1.462
    8. Storage Temp.: 2-8°C
    9. Solubility: DMSO (Slightly), Ethyl Acetate (Slightly)
    10. CAS DataBase Reference: 8-BROMOOCTANOIC ACID ETHYL ESTER(CAS DataBase Reference)
    11. NIST Chemistry Reference: 8-BROMOOCTANOIC ACID ETHYL ESTER(29823-21-0)
    12. EPA Substance Registry System: 8-BROMOOCTANOIC ACID ETHYL ESTER(29823-21-0)

  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 29823-21-0(Hazardous Substances Data)

29823-21-0 Usage

Description

8-BROMOOCTANOIC ACID ETHYL ESTER, also known as Ethyl 8-bromooctanoate, is an organic compound that serves as a valuable research reagent in the field of organic synthesis and other chemical processes. It is characterized by its unique chemical structure and properties, which make it a versatile compound for various applications.

Uses

Used in Organic Synthesis:
8-BROMOOCTANOIC ACID ETHYL ESTER is used as a research reagent for its role in organic synthesis. It is particularly valuable in the development and synthesis of new organic compounds, contributing to the advancement of chemical research and innovation.
Used in Chemical Processes:
In addition to its role in organic synthesis, 8-BROMOOCTANOIC ACID ETHYL ESTER is also utilized in various chemical processes. Its unique properties make it a useful component in the development and optimization of different chemical procedures, further expanding its applications in the field of chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 29823-21-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,8,2 and 3 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 29823-21:
(7*2)+(6*9)+(5*8)+(4*2)+(3*3)+(2*2)+(1*1)=130
130 % 10 = 0
So 29823-21-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H19BrO2/c1-2-13-10(12)8-6-4-3-5-7-9-11/h2-9H2,1H3

29823-21-0SDS

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 8-bromooctanoate

1.2 Other means of identification

Product number -
Other names Ethyl 8-bromoocatanoate

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:29823-21-0 SDS

29823-21-0Relevant articles and documents

Ti-catalyzed homolytic opening of ozonides: A sustainable C-C bond-forming reaction

Rosales, Antonio,Munoz-Bascon, Juan,Lopez-Sanchez, Cristobal,Alvarez-Corral, Miriam,Munoz-Dorado, Manuel,Rodriguez-Garcia, Ignacio,Oltra, J. Enrique

, p. 4171 - 4176 (2012/06/18)

The unprecedented homolytic opening of ozonides promoted and catalyzed by titanocene(III) is reported. This novel reaction proceeds at room temperature under neutral, mild conditions compatible with many functional groups and provides carbon radicals suitable to form C-C bonds via both homocoupling and cross-coupling processes. The procedure has been advantageously exploited for the straightforward synthesis of the natural product brittonin A.

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