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Showing content from https://en.wikipedia.org/wiki/Sinapyl_alcohol below:

Sinapyl alcohol - Wikipedia

From Wikipedia, the free encyclopedia

4-[(1E)-3-Hydroxyprop-1-en-1-yl]-2,6-dimethoxyphenol

Sinapoyl alcohol, 4-Hydroxy-3,5-dimethoxycinnamyl alcohol

• 537-33-7 ^Y

3D model (

)

• Interactive image

• CHEBI:64557 ^N

• 4444145 ^N

• C02325 ^N

• 5280507

• 8O6NO04SMV ^Y

• DTXSID501314695 DTXSID10895025, DTXSID501314695

• InChI=1S/C11H14O4/c1-14-9-6-8(4-3-5-12)7-10(15-2)11(9)13/h3-4,6-7,12-13H,5H2,1-2H3/b4-3+

   ^N

  Key: LZFOPEXOUVTGJS-ONEGZZNKSA-N

   ^N

• OC/C=C/c1cc(OC)c(O)c(OC)c1

Except where otherwise noted, data are given for materials in their

(at 25 °C [77 °F], 100 kPa).

(

?)

Chemical compound

Sinapyl alcohol is an organic compound structurally related to cinnamic acid. It is biosynthetized via the phenylpropanoid biochemical pathway, its immediate precursor being sinapaldehyde. This phytochemical is one of the monolignols, which are precursor to lignin or lignans.^[1] It is also a biosynthetic precursor to various stilbenoids and coumarins.

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