Pharmaceutical intermediates

Home - Products - Pharmaceutical intermediates

Ethyl (2S)-2-bromopropanoate

  • Product Name: Ethyl (2S)-2-bromopropanoate
  • CasNo: 535-11-5
  • Purity:
  • Appearance: clear colorless to very slightly yellow liquid

Mobile/Wechat/WhatsApp: Chen Shihuai +86-13961989018  Yang Zhengquan +86-13921613169   Chen Yi +86-13962066393

Email:

Inquiry

CasNo: 535-11-5

Molecular Formula: C5H9BrO2

Appearance: clear colorless to very slightly yellow liquid

Excellent chemical plant bulk supply Ethyl (2S)-2-bromopropanoate 535-11-5

  • Molecular Formula:C5H9BrO2
  • Molecular Weight:181.029
  • Appearance/Colour:clear colorless to very slightly yellow liquid 
  • Vapor Pressure:2.15mmHg at 25°C 
  • Melting Point:<25 °C 
  • Refractive Index:n20/D 1.446(lit.)  
  • Boiling Point:162.6 °C at 760 mmHg 
  • Flash Point:58.4 °C 
  • PSA:26.30000 
  • Density:1.413 g/cm3 
  • LogP:1.33290 

Ethyl 2-bromopropionate(Cas 535-11-5) Usage

Chemical Description

Ethyl 2-bromopropionate is a chemical compound with the molecular formula C5H9BrO2.

Purification Methods

Wash the ester with saturated aqueous Na2CO3 (three times), 50% aqueous CaCl2 (three times) and saturated aqueous NaCl (twice). Dry with MgSO4, CaCl2 or CaCO3, and distil it. [Beils

InChI:InChI=1/C5H9BrO2/c1-3-8-5(7)4(2)6/h4H,3H2,1-2H3/t4-/m1/s1

535-11-5 Relevant articles

Acridine Orange Hemi(Zinc Chloride) Salt as a Lewis Acid-Photoredox Hybrid Catalyst for the Generation of α-Carbonyl Radicals

Das, Sanju,De Sarkar, Suman,Mandal, Tanumoy

supporting information, (2021/12/10)

A readily accessible organic-inorganic h...

Regio- and Stereoselective Nickel-Catalyzed Coupling of Boronic Acids with Allenoates

Liu, Yang,Daka, Mario,Bandini, Marco

, p. 3187 - 3196 (2018/08/17)

The Ni(II)-catalyzed cross-coupling of a...

Synthesis of [13C3]-B6 vitamers labelled at three consecutive positions starting from [13C3]-propionic acid

Bachmann, Thomas,Rychlik, Michael

, (2018/09/11)

[13C3]-labelled vitamers (PN, PL and PM)...

Prototypic 18F-Labeled Argininamide-Type Neuropeptide Y Y1R Antagonists as Tracers for PET Imaging of Mammary Carcinoma

Keller, Max,Maschauer, Simone,Brennauer, Albert,Tripal, Philipp,Koglin, Norman,Dittrich, Ralf,Bernhardt, Günther,Kuwert, Torsten,Wester, Hans-Jürgen,Buschauer, Armin,Prante, Olaf

supporting information, p. 304 - 309 (2017/03/17)

The neuropeptide Y (NPY) Y1 receptor (Y1...

535-11-5 Process route

ethanol
64-17-5

ethanol

2-Bromopropionic acid
598-72-1,10327-08-9

2-Bromopropionic acid

Ethyl 2-bromopropionate
535-11-5,41978-69-2

Ethyl 2-bromopropionate

Conditions
Conditions Yield
With Dowex 50 X8; In toluene; for 5.5h; Dean-Stark; Reflux;
76%
With hydrogenchloride; In diethyl ether;
75%
With dmap; dicyclohexyl-carbodiimide; In diethyl ether; at 25 ℃; for 3h; Inert atmosphere;
72%
With hydrohalic acid;
With sulfuric acid;
Acidic conditions;
ethanol
64-17-5

ethanol

α-bromopropionyl bromide
563-76-8

α-bromopropionyl bromide

Ethyl 2-bromopropionate
535-11-5,41978-69-2

Ethyl 2-bromopropionate

Conditions
Conditions Yield
With pyridine; In chloroform; at 0 ℃; for 1h;
With pyridine; In dichloromethane;
In ethyl acetate; at 20 ℃; for 3h;
With triethylamine; In dichloromethane; at 0 - 20 ℃;
With pyridine; In dichloromethane; at 0 - 20 ℃;

535-11-5 Upstream products

  • 64-17-5
    64-17-5

    ethanol

  • 563-76-8
    563-76-8

    α-bromopropionyl bromide

  • 97-64-3
    97-64-3

    ethyl 2-hydroxypropionate

  • 598-72-1
    598-72-1

    2-Bromopropionic acid

535-11-5 Downstream products

  • 63909-12-6
    63909-12-6

    2-piperidino-propionic acid ethyl ester

  • 32418-62-5
    32418-62-5

    (morpholinyl-4)-2 propanoate d'ethyle

  • 100058-86-4
    100058-86-4

    ethyl 3-(5-methylfuran-2-yl)-2-methylacrylate

  • 609-14-3
    609-14-3

    2-acetylpropanoic acid ethyl ester

Leave Your Message

Relevant Products