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CS-W001157 4
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Methyl 3,5-bis(hydroxymethyl)benzoate

  • CAS No. 193953-02-5

  • Cat. No. CS-0149867
  • Molecule weightNone
  • Purity≥98%
  • MDL No.MFCD28365129

*For research and further manufacturing use only, not for direct human use.

Methyl 3,5-bis(hydroxymethyl)benzoate|CS-0149867

Structure of 193953-02-5

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General Information

  • CAS No. 193953-02-5
  • Cat. No. CS-0149867
  • Purity ≥98%
  • MDL No. MFCD28365129
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₀H₁₂O₄
  • Molecular Weight None
  • Synonym(s) 3,5-bis(hydroxylmethyl)benzoic acid methyl ester
  • SMILES O=C(C1=CC(=CC(=C1)CO)CO)OC

Description

Methyl 3,5-bis(hydroxymethyl)benzoate features two hydroxymethyl groups flanking a methyl ester on a benzene ring, enabling dual functionalization in synthetic sequences. This bench-stable, moisture-tolerant reagent integrates readily into polyfunctional architectures, serving as a key building block for bioactive scaffolds and advanced materials.

Application

Methyl 3,5-bis(hydroxymethyl)benzoate serves as a versatile diol-containing aromatic building block, enabling efficient functionalization at both ortho positions relative to the ester. The two primary hydroxymethyl groups facilitate selective oxidation, protection, or coupling reactions, supporting applications in medicinal chemistry and materials synthesis. Its bench-stable nature and compatibility with standard purification methods make it well-suited for multi-step synthetic workflows.

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P260-P264-P270-P271-P280-P301+P310-P302+P352-P304+P340-P305+P351+P338-P312-P330-P332+P313-P337+P313-P362+P364-P403+P233-P405-P501

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Computational Chemistry Data

  • TPSA   66.76
  • LogP   0.4578
  • H_Acceptors   4
  • H_Donors   2
  • Rotatable_Bonds   3

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