123-11-5,4-methoxybenzaldehyde, Page 14 suppliers
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CAS No 123-11-5 , 4-methoxybenzaldehyde

  • Name: 4-methoxybenzaldehyde
  • Synonyms: Benzaldehyde; Anisaldehyde; 4-Anisaldehyde;4-Methoxybenzaldehyde; P-ANISALDEHYDE; 4-methoxy-; 123-11-5;4-methoxybenzaldehyde; p-Methoxybenzaldehyde; Anisic aldehyde; Aubepine;
  • CAS Registry Number:
  • Transport: 225kgs
  • Melting Point: -1 ºC
  • Flash Point: 116 ºC
  • Boiling Point: 248-249 ºC
  • Density: 1.121
  • Refractive index: 1.571-1.574
  • Water Solubility: Insoluble (soluble in alcohol, ether)
  • Safety Statements: R22
  • Hazard Symbols: Xn: Harmful;
  • HS Code: 29124900
  • Flash Point: 116 ºC
  • EINECS: 204-602-6
  • Molecular Weight: 136.14792
  • InchiKey: ZRSNZINYAWTAHE-UHFFFAOYSA-N
  • InChI: InChI=1S/C8H8O2/c1-10-8-4-2-7(6-9)3-5-8/h2-6H,1H3
  • Risk Statements: R22
  • Molecular Formula: C8H8O2
  • Molecular Structure:CAS No:123-11-5 4-methoxybenzaldehyde

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References of 4-methoxybenzaldehyde
Title: p-Anisaldehyde
CAS Registry Number: 123-11-5
CAS Name: 4-Methoxybenzaldehyde
Synonyms: anisic aldehyde
Molecular Formula: C8H8O2
Molecular Weight: 136.15
Percent Composition: C 70.57%, H 5.92%, O 23.50%
Literature References: Metabolic product of the odoriferous fungus Lentinus lepidus Fr.: Birkinshaw et al., Biochem. J. 38, 131 (1944); of wood-rotting fungus Polyporus benzoinus (Wahl.) Fr.: Birkinshaw et al., ibid. 50, 509 (1952); of Daldalea juniperina Murr.: Birkinshaw, Chaplen, ibid. 60, 255 (1955). Prepn: Niedzielski, Nord, J. Am. Chem. Soc. 63, 1462 (1941); Sisti et al., J. Org. Chem. 27, 279 (1962). Toxicity study: P. M. Jenner et al., Food Cosmet. Toxicol. 2, 327 (1964).
Properties: Oily liquid, bp 248°, bp1.5 89-90°. mp 0°. d415 1.119. nD13 1.5764. Volatile in steam. Very slightly sol in water; misc with alc, ether. LD50 orally in rats: 1510 mg/kg (Jenner).
Melting point: mp 0°
Boiling point: bp 248°; bp1.5 89-90°
Index of refraction: nD13 1.5764
Density: d415 1.119
Toxicity data: LD50 orally in rats: 1510 mg/kg (Jenner)
Use: Perfumery and toilet soaps; odor resembles that of coumarin, but the aldehyde must be mixed with other odorous substances to yield an agreeable odor. Also used in organic syntheses.