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Ethyl 2-bromopropionate - 99%, high purity , CAS No.535-11-5

    Grade & Purity:
  • ≥99%
In stock
Item Number
E400066
Grouped product items
SKU Size
Availability
Price Qty
E400066-25g
25g
7
$23.90
E400066-100g
100g
3
$49.90
E400066-500g
500g
1
$138.90
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Organic building blocks (409)

Basic Description

Synonyms (+/-)-ETHYL .ALPHA.-BROMOPROPIONATE | 2-bromopropionic acid ethylester | EINECS 255-601-2 | ETHYL .ALPHA.-BROMOPROPIONATE [MI] | .alpha.-Bromopropionic acid ethyl ester | Ethyl (1)-2-bromopropionate | ethyl 2-bromoproionate | Ethyl 2-bromopropanoate | eth
Specifications & Purity ≥99%
Storage Temp Protected from light
Shipped In Normal

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organic acids and derivatives
Class Carboxylic acids and derivatives
Subclass Alpha-halocarboxylic acids and derivatives
Intermediate Tree Nodes Not available
Direct Parent Alpha-halocarboxylic acid derivatives
Alternative Parents Carboxylic acid esters  Monocarboxylic acids and derivatives  Organobromides  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  Alkyl bromides  
Molecular Framework Aliphatic acyclic compounds
Substituents Alpha-halocarboxylic acid derivative - Carboxylic acid ester - Monocarboxylic acid or derivatives - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organobromide - Organohalogen compound - Carbonyl group - Alkyl halide - Alkyl bromide - Aliphatic acyclic compound
Description This compound belongs to the class of organic compounds known as alpha-halocarboxylic acid derivatives. These are carboxylic acid derivatives containing a halogen atom bonded to the alpha carbon atom.
External Descriptors Not available

Names and Identifiers

Pubchem Sid 504755338
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504755338
IUPAC Name ethyl 2-bromopropanoate
INCHI InChI=1S/C5H9BrO2/c1-3-8-5(7)4(2)6/h4H,3H2,1-2H3
InChIKey ARFLASKVLJTEJD-UHFFFAOYSA-N
Smiles CCOC(=O)C(C)Br
Isomeric SMILES CCOC(=O)C(C)Br
WGK Germany 3
RTECS UA2451730
UN Number 2920
Packing Group II
Molecular Weight 181.03
Beilstein 773920
Reaxy-Rn 773920
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=773920&ln=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

17 results found

Lot Number Certificate Type Date Item
H2301539 Certificate of Analysis May 07, 2025 E400066
H2301542 Certificate of Analysis May 07, 2025 E400066
H2301558 Certificate of Analysis May 07, 2025 E400066
H2301562 Certificate of Analysis May 07, 2025 E400066
H2301575 Certificate of Analysis May 07, 2025 E400066
H2301557 Certificate of Analysis May 07, 2025 E400066
D2304497 Certificate of Analysis Jan 15, 2025 E400066
D2312015 Certificate of Analysis Jan 07, 2025 E400066
D2429245 Certificate of Analysis Apr 12, 2024 E400066
D2429244 Certificate of Analysis Apr 12, 2024 E400066
D2429246 Certificate of Analysis Apr 12, 2024 E400066
F2526014 Certificate of Analysis Apr 12, 2024 E400066
D2228017 Certificate of Analysis Feb 21, 2024 E400066
D2228022 Certificate of Analysis Feb 21, 2024 E400066
H2301529 Certificate of Analysis Jul 07, 2023 E400066
D2228018 Certificate of Analysis Mar 02, 2022 E400066
D2228019 Certificate of Analysis Mar 02, 2022 E400066

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Chemical and Physical Properties

Solubility Immiscible in water. Soluble in alcohol and ether.
Sensitivity light sensitive
Refractive Index 1.449
Flash Point(°F) 123.8 °F
Flash Point(°C) 51℃
Boil Point(°C) 156-160°C
Molecular Weight 181.030 g/mol
XLogP3 1.700
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 2
Rotatable Bond Count 3
Exact Mass 179.979 Da
Monoisotopic Mass 179.979 Da
Topological Polar Surface Area 26.300 Ų
Heavy Atom Count 8
Formal Charge 0
Complexity 82.500
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 1
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

Citations of This Product

1. Man Zhang, Rubo Tian, Siyang Tang, Kejing Wu, Binshen Wang, Yingying Liu, Yingming Zhu, Houfang Lu, Bin Liang.  (2023)  The structure and properties of lignin isolated from various lignocellulosic biomass by different treatment processes.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,  243  (125219). 
2. Xue Tao, Wei Yan, Yu Caili, Zhou Zhongqun, Zhang Faai.  (2023)  RAFT polymerization of MMA in channels of different mesoporous materials.  CHEMICAL PAPERS,  77  (7): (3713-3726). 
3. Tian Wang, Boya Hao, Shilin Xu, Jie Meng, Tao Wen, Jian Liu, Haiyan Xu.  (2022)  Effective RNAi in leukemia cells is enhanced by spermine-modified pullulan combined with desloratadine.  CARBOHYDRATE POLYMERS,  292  (119646). 
4. Xu Xiang, Zeng Yanning, Yu Caili, Zhang Faai.  (2020)  Controlled RAFT polymerization of MMA in confined space of various pore sizes of SBA-15.  JOURNAL OF POROUS MATERIALS,  27  (1): (95-105). 
5. Yuan Wang, Yan-Ling Luo, Feng Xu, Ya-Shao Chen, Wei Tang.  (2017)  Redox-responsive PAEFc-b-PDMAEMA amphiphilic block copolymer self-assembly micelles: Physicochemical properties and anticancer drug controlled release.  JOURNAL OF INDUSTRIAL AND ENGINEERING CHEMISTRY,  48  (66). 
6. Deng Jun, Wu Sai, Yao Mengyun, Gao Changyou.  (2016)  Surface-anchored poly(acryloyl-L(D)-valine) with enhanced chirality-selective effect on cellular uptake of gold nanoparticles.  Scientific Reports,  (1): (1-12). 
7. Sai Chen,Yue Yu,Ruirui Cao,Haihui Liu,Xingxiang Zhang.  (2019-07-04)  Fabrication and Characterization of Novel Shape-Stabilized Phase Change Materials Based on P(TDA-co-HDA)/GO Composites..  Polymers,  11  ((7)):  
8. Jian Guan, Xiaodi Yu, Minghui He, Wenfeng Han, Ying Li, Zongjian Liu, Panpan Zhang, Haodong Tang.  (2024)  Synthesis of Ultrahigh Molecular Weight Poly (Trifluoroethyl Methacrylate) Initiated by the Combination of Palladium Nanoparticles with Organic Halides.  Polymers,  16  (19): (2764). 

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