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CAS 29169-64-0

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O-Formyl-D-mandeloyl chloride

Description:
O-Formyl-D-mandeloyl chloride, with the CAS number 29169-64-0, is an organic compound characterized by its functional groups and structural features. It is a derivative of mandelic acid, which is known for its chiral properties and is often utilized in the synthesis of various pharmaceuticals and agrochemicals. The presence of the formyl group (-CHO) indicates that it can participate in further chemical reactions, such as nucleophilic additions or condensation reactions. The chloride substituent suggests that it can act as a reactive electrophile, making it useful in acylation reactions. This compound is typically a colorless to pale yellow liquid or solid, depending on its purity and specific conditions. It is important to handle it with care due to its reactivity and potential hazards associated with chlorinated compounds. In terms of solubility, it is generally soluble in organic solvents, which facilitates its use in various synthetic applications. Overall, O-Formyl-D-mandeloyl chloride is a valuable intermediate in organic synthesis, particularly in the development of chiral compounds.
Formula:C9H7ClO3
InChI:InChI=1S/C9H7ClO3/c10-9(12)8(13-6-11)7-4-2-1-3-5-7/h1-6,8H/t8-/m1/s1
InChI key:InChIKey=ZNLABNPTWSKGDX-MRVPVSSYSA-N
SMILES:[C@H](OC=O)(C(Cl)=O)C1=CC=CC=C1
Synonyms:
  • (-)-O-Formyl-<span class="text-smallcaps">D</span>-mandeloyl chloride
  • (1R)-2-chloro-2-oxo-1-phenylethyl formate
  • (D)-(-)-O-formylmandeloyl chloride
  • (R)-(-)-Alpha-(Formyloxy)Phenylacetyl Chloride
  • (R)-Alpha-(Chlorocarbonyl)Benzyl Formate
  • (αR)-α-(Formyloxy)benzeneacetyl chloride
  • 2-Chloro-2-Oxo-1-Phenylethyl Formate
  • <span class="text-smallcaps">D</span>-Phenyl(formyloxy)acetyl chloride
  • Alpha-Formylmandeloyl Chloride
  • Benzeneacetyl chloride, α-(formyloxy)-, (R)-
  • See more synonyms
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