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(S)-(-)-2-Acetoxypropionyl chloride

Base Information Edit
  • Chemical Name:(S)-(-)-2-Acetoxypropionyl chloride
  • CAS No.:36394-75-9
  • Molecular Formula:C5H7ClO3
  • Molecular Weight:150.562
  • Hs Code.:2918199890
  • European Community (EC) Number:420-610-4,609-239-0
  • DSSTox Substance ID:DTXSID00454923
  • Nikkaji Number:J1.060.097I
  • Wikidata:Q72434394
  • Mol file:36394-75-9.mol
(S)-(-)-2-Acetoxypropionyl chloride

Synonyms:(S)-(-)-2-Acetoxypropionyl chloride;36394-75-9;(S)-(-)-2-acetoxypropionylchloride;[(2S)-1-chloro-1-oxopropan-2-yl] acetate;(S)-1-chloro-1-oxopropan-2-yl acetate;(S)-2-acetoxypropanyl chloride;(1S)-2-chloro-1-methyl-2-oxoethyl acetate;(S)-2-acetoxypropionyl chloride;S-2-ACETOXYPROPIONYL CHLORIDE;MFCD00145252;(2S)-1-chloro-1-oxopropan-2-yl acetate;EC 420-610-4;Mosandl reagent;SCHEMBL76020;(R)-(-)-2-mandelic acid;2(S)-acetoxypropionyl chloride;S-2-Acetoxy propionyl chloride;DTXSID00454923;ALHZEIINTQJLOT-VKHMYHEASA-N;BCP04460;(S)-(-)-O-Acetyllactoyl Chloride;O-Acetyl-L-lactyl chloride, AP-Cl;(S)-2-(Acetyloxy)propanoyl chloride;AKOS015900495;(S)-(-)-2-acetoxy-propionyl chloride;AS-38669;(25)-1-chloro-1-oxopropan-2-yl acetate;()-(-)-2-ACETOXYPROPIONYL CHLORIDE;A1297;(S)-(-)-2-Acetoxypropionyl chloride, 97%;(S)-acetic acid 1-chlorocarbonyl-ethyl ester;acetic acid (S)-1-chlorocarbonyl-ethyl ester;[(1S)-2-Chloro-1-methyl-2-oxoethyl] acetate;[(1S)-2-Chloro-1-methyl-2-oxo-ethyl] acetate;A823225;(S)-(-)-2-Acetoxypropionyl chloride, for chiral derivatization, >=99.0%

Suppliers and Price of (S)-(-)-2-Acetoxypropionyl chloride
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • L-α-AcetoxypropionylChloride
  • 1g
  • $ 50.00
  • TCI Chemical
  • (S)-(-)-2-Acetoxypropionyl Chloride >97.0%(GC)(T)
  • 5g
  • $ 125.00
  • TCI Chemical
  • (S)-(-)-2-Acetoxypropionyl Chloride >97.0%(GC)(T)
  • 1g
  • $ 42.00
  • SynQuest Laboratories
  • (2S)-(-)-2-Acetoxypropanoyl chloride
  • 1 g
  • $ 50.00
  • SynQuest Laboratories
  • (2S)-(-)-2-Acetoxypropanoyl chloride
  • 5 g
  • $ 128.00
  • Sigma-Aldrich
  • (S)-(?)-2-Acetoxypropionyl chloride 97%
  • 5g
  • $ 131.00
  • Apolloscientific
  • (2S)-(-)-2-Acetoxypropanoylchloride
  • 1g
  • $ 45.00
  • Ambeed
  • (S)-(-)-2-Acetoxypropionyl Chloride 98%
  • 25g
  • $ 627.00
  • Ambeed
  • (S)-(-)-2-Acetoxypropionyl Chloride 98%
  • 1g
  • $ 43.00
Total 106 raw suppliers
Chemical Property of (S)-(-)-2-Acetoxypropionyl chloride Edit
Chemical Property:
  • Appearance/Colour:Colorless fuming liquids 
  • Vapor Pressure:2.022mmHg at 25°C 
  • Refractive Index:n20/D 1.423(lit.)  
  • Boiling Point:163.862 °C at 760 mmHg 
  • Flash Point:62.593 °C 
  • PSA:43.37000 
  • Density:1.22 g/cm3 
  • LogP:0.70340 
  • Storage Temp.:2-8°C 
  • XLogP3:1.1
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:3
  • Exact Mass:150.0083718
  • Heavy Atom Count:9
  • Complexity:132
Purity/Quality:

98% *data from raw suppliers

L-α-AcetoxypropionylChloride *data from reagent suppliers

Safty Information:
  • Pictogram(s): Corrosive
  • Hazard Codes:
  • Statements: 34-43-22 
  • Safety Statements: 26-36/37/39-45-23 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(C(=O)Cl)OC(=O)C
  • Isomeric SMILES:C[C@@H](C(=O)Cl)OC(=O)C
  • Uses Frequently used chiral building block. Also used to resolve a bicyclic α-hydroxylactone and to prepare chiral phosphonates used in an enantiomeric excess assay of unprotected amino acids. Useful chiral derivatizing agent.
Technology Process of (S)-(-)-2-Acetoxypropionyl chloride

There total 8 articles about (S)-(-)-2-Acetoxypropionyl chloride which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With thionyl chloride; at 50 ℃; for 2h;
Guidance literature:
Guidance literature:
With hydrogenchloride; thionyl chloride; In diethyl ether;
DOI:10.3987/COM-98-S(H)60
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