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Detail of "14615-72-6"

  • CAS Number:
  • 14615-72-6
  • Name:
  • Benzaldehyde,3,5-bis(phenylmethoxy)-

  • Superlist Name:
  • 3,5-Dibenzyloxybenzaldehyde
  • Molecular Structure:
  • Formula:
  • C21H18O3
  • Molecular Weight:
  • 318.37
  • Synonyms:
  • Benzaldehyde,3,5-bis(benzyloxy)- (8CI);3,5-Bis(benzyloxy)benzaldehyde;3,5-Bis(phenylmethoxy)benzaldehyde;
  • Density:
  • 1.176 g/cm3
  • Melting Point:
  • 78-80 °C(lit.)
  • Boiling Point:
  • 502.4 °C at 760 mmHg
  • Flash Point:
  • 250 °C
  • Appearance:
  • orange to orange-tan powder or crystalline powder

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CAS No.14615-72-6 3,5-DibenzyloxybenzaldehydeCompetitive Product

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Supplier:Jiangsu Changzhou Qiangda Baocheng Chemical Technical Institute [ China (Mainland)]

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CAS No.14615-72-6 3,5-Dibenzyloxybenzaldehyde

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CAS No.14615-72-6 3,5-Dibenzyloxybenzaldehyde

Supplier:ChemOrganic Limited [ China (Mainland)]

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CAS No.14615-72-6 3,5-Dibenzyloxybenzaldehyde

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CAS No.14615-72-6 3,5-Dibenzyloxybenzaldehyde

3,5-Dibenzyloxybenzaldehyde

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CAS No.14615-72-6 3,5-Dibenzyloxybenzaldehyde

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CAS No.14615-72-6 3,5-Dibenzyloxybenzaldehyde

Supplier:ratiochem GmbH [ Germany]

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CAS No.14615-72-6 3,5-Dibenzyloxybenzaldehyde

Supplier:hangzhou dimachema intermediate co.ltd. [ China (Mainland)]

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Reference

Synthesis of cannabinoid model compounds
Synthesis of cannabinoid model compounds. Part 3. (6aR, 10aR)-N-Ethyl-D8-tetrahydrocannabinol-18-amide, (6aR, 10aR, 17RS)-N-ethyl-17-methyl-D8-tetrahydrocannabinol-18-amide and (6aR, 10aR)-17,18-didehydro-D8-tetrahydrocannabinol. Schmidt, Burkhard; Franke, Ingo; Witteler, Franz Josef; Binder, Michael (Inst. Physiol. Chem., Ruhr-Univ. Bochum, Bochum D-4630/1, Fed. Rep. Ger.). Helv. 14615-72-6 and 58545-34-9 are cas registry numbers of chemicals which are used as reagents here. Chim. Acta, 66(8), 2564-71 (English) 1983. CODEN: HCACAV. ISSN: 0018-019X. DOCUMENT TYPE: Journal CA Section: 30 (Terpenes and Terpenoids) Cannabinoids I (R = H, Me; R1 = NHEt) were prepd. via Wittig condensation of 3,5-(PhCH2O)2C6H3CHO with MeO2CCHRCH2CH2P+Ph3I- and treatment of the (acyloxy)succinimides I (R = H, Me; R1 = succinimidooxy) with EtNH2. Moreover, the synthetic cannabinoid II (R2 = CH:CH2) was selectively deuterated to give II (R2 = CHDCH2D). .
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