2,3-Dichloro-1-propene, 98%
2,3-Dichloro-1-propene, 98%
2,3-Dichloro-1-propene, 98%
Thermo Scientific Chemicals

2,3-Dichloro-1-propene, 98%

CAS: 78-88-6 | C3H4Cl2 | 110.965 g/mol
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產品號碼 L08943.30
亦稱為 L08943-30
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250 g
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化學識別
CAS78-88-6
IUPAC Name2,3-dichloroprop-1-ene
Molecular FormulaC3H4Cl2
InChI KeyFALCMQXTWHPRIH-UHFFFAOYSA-N
SMILESClCC(Cl)=C
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規格Specification Sheet規格表
Appearance (Color)Clear colorless to pale yellow to pale brown
Assay (GC)≥97.5%
FormLiquid
Refractive Index1.4595-1.4635 @ 20?C
It is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
It is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff.

Solubility
Soluble in water (2g/L).

Notes
Store in cool. Keep container tightly closed in a dry and well-ventilated place. Store away from oxidizing agent.
RUO – Research Use Only

General References:

  1. T Neudecker and D Henschler. Mutagenicity of chloroolefins in the Salmonella/mammalian microsome test. III. Metabolic activation of the allylic chloropropenes allyl chloride, 1,3-dichloropropene, 2,3-dichloro-1-propene, 1,2,3-trichloropropene, 1,1,2,3-tetrachloro-2-propene and hexachloropropene by S9 mix via two different metabolic pathways. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis,1986, 107 (1-2), 1-9.
  2. Roland P H Schmitz et. al. Evidence for a radical mechanism of the dechlorination of chlorinated propenes mediated by the tetrachloroethene reductive dehalogenase of Sulfurospirillum muftivorans. Environmental Science & Technology. 2007, 41 (21), 7370-7375.
  3. Reductive elimination with Zn powder gives allene free from methylacetylene: Org. Synth. Coll., 5, 22 (1973).
  4. Electron-acceptor, with concomitant reduction to allene, in a high-yield coupling of aryl Grignard reagents to symmetrical biaryls: Tetrahedron Lett., 29, 1293 (1988):