2,5-Dimethxybenzaldehyde CAS#93-02-7

Core Building Block for Organic Synthesis: 2,5‑Dimethoxybenzaldehyde serves as a vital intermediate extensively adopted in diverse organic synthetic routes.

Targeted Synthetic Utility: It holds notable value for manufacturing 2,5‑dimethoxyphenethylamine (2C‑H) and its derivative analogues.

Predictable Solid Characteristics: This compound occurs as crystals with a melting point ranging from 49 to 51°C, supporting stable and repeatable processing operations.

Low Aqueous Affinity for Custom Reaction Designs: It cannot dissolve in water, making it well suited for reaction systems that demand minimal compatibility with aqueous media.

Product Description of 2,5‑Dimethoxybenzaldehyde CAS#93‑02‑7 2,5‑Dimethoxybenzaldehyde (CAS#93‑02‑7) presents as yellow crystalline solid. It acts as an intermediate for organic‑synthesis workflows, and is especially important for manufacturing 2,5‑dimethoxyphenethylamine (2C‑H) and its related derivative compounds. It has a molecular weight of 166.18, a melting point of 49‑51 °C, and exhibits no solubility in water.1773984739789020.jpg.webp

2,5-Dimethoxybenzaldehyde Chemical Properties

Melting point 46-48 °C (lit.)
Boiling point 146 °C/10 mmHg (lit.)
density 1.1708 (rough estimate)
refractive index 1.5260 (estimate)
Fp >230 °F
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility 795mg/l
form Crystalline Powder, Crystals and/or Chunks
color Yellow to beige
Water Solubility Soluble in chloroform and methanol. Slightly soluble in water.
Sensitive Air Sensitive
BRN 509301
InChIKeyAFUKNJHPZAVHGQ-UHFFFAOYSA-N
LogP1.91
CAS DataBase Reference93-02-7(CAS DataBase Reference)
NIST Chemistry ReferenceBenzaldehyde, 2,5-dimethoxy-(93-02-7)
EPA Substance Registry SystemBenzaldehyde, 2,5-dimethoxy- (93-02-7)
Hazard Codes Xi
Risk Statements 36/37/38-43
Safety Statements 26-36/37/39-24/25-36
WGK Germany 2
RTECS CU5740500
Hazard Note Irritant
TSCA Yes
HS Code 29124900

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Product Application of 2,5-Dimethoxybenzaldehyde CAS#93-02-7 Phenethylamine Derivative Precursor It serves as a starting material for the synthesis of substituted phenethylamine derivatives within academic and chemical research.

Laboratory Synthetic Building Block It is widely adopted as a versatile intermediate for general organic synthesis research.1773984756987568.jpg.webp

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