Olivetol
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Olivetol ??
- ???
- 46-48 °C(lit.)
- ?? ?
- 164 °C
- ??
- 1.068±0.06 g/cm3(Predicted)
- ???
- >230 °F
- ?? ??
- Keep in dark place,Inert atmosphere,Room temperature
- ???
- ?????(?? ???), ???(?? ???)
- ??? ??
- ??
- ??? ??
- ??? ??
- ?? ?? (pKa)
- 9.59±0.10(Predicted)
- ??
- ??~????
- ???
- ???
- InChI
- InChI=1S/C11H16O2/c1-2-3-4-5-9-6-10(12)8-11(13)7-9/h6-8,12-13H,2-5H2,1H3
- InChIKey
- IRMPFYJSHJGOPE-UHFFFAOYSA-N
- SMILES
- C1(O)=CC(CCCCC)=CC(O)=C1
- CAS ??????
- 500-66-3(CAS DataBase Reference)
??
- ?? ? ?? ??
- ?? ? ???? ?? (GHS)
| ??? ?? | Xi | ||
|---|---|---|---|
| ?? ???? ?? | 36/37/38 | ||
| ????? | 26-36/39 | ||
| WGK ?? | 3 | ||
| RTECS ?? | VH2880000 | ||
| HS ?? | 2907290090 | ||
| ???? ??? | 6.1C - Combustible acute toxic Cat.3 toxic compounds or compounds which causing chronic effects |
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| Hazard Classifications | Acute Tox. 4 Oral Aquatic Acute 1 Aquatic Chronic 3 Eye Dam. 1 Skin Irrit. 2 Skin Sens. 1B STOT SE 1 Oral STOT SE 2 Oral |
| ????(GHS): |
  
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| ?? ?: | Danger | |||||||||||||||||||||||||||||||||||
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Olivetol C??? ??, ??, ??
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Olivetol is an off-white crystals or olive to light purple waxy solid. Forms monohydrate (melting point: 102-106°F). Olivetol is a member of the class of resorcinols that is resorcinol in which the hydrogen at position 5 is replaced by a pentyl group. It has a role as a lichen metabolite.??? ??
light purple to brown crystalline mass.?? ??
Olivetol is a precursor in various syntheses of tetrahydrocannabinol.??
Olivetol was used as a template molecule in the synthesis of molecularly imprinted polymer (MIP). It was also used as an inhibitor of (S)-mephenytoin 4'-hydroxylase activity of recombinant CYP2C19.??
ChEBI: Olivetol is a member of the class of resorcinols that is resorcinol in which the hydrogen at position 5 is replaced by a pentyl group. It has a role as a lichen metabolite.?? ??
olivetol can also be formed through hydrolysis of intermediate polyketide CoAs or spontaneous cyclization.
?? ??
Olivetol appears as off-white crystals or olive to light purple waxy solid. Forms monohydrate (melting point: 102-106°F). (NTP, 1992)??? ?? ??
Sensitive to air. Insoluble in water.?? ???
Olivetol is incompatible with acid chlorides, acid anhydrides and oxidizing agents.????
Olivetol is probably combustible.???? ??
Olivetol (5-Pentylresorcinol, 5-n-Amylresorcinol) is a naturally occurring organic compound being a precursor in various syntheses of tetrahydrocannabinol. It acts as a competitive inhibitor of the cannabinoid receptors CB1 and CB2.Safety
Olivetol is still a very new product. It has not been researched nearly enough to prove it's safe to use. So far, no one has reported any adverse side effects as far as we know. Until more information is available, carefully control your THC intake instead of relying on an untested gelcap.Olivetol ?? ?? ? ???
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??(3-)-2-?
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????(???)
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Benzenemethanol, α-butyl-3,5-bis(phenylmethoxy)-
3,5-Bis(benzyloxy)benzoic acid benzyl ester
methyl 6-n-pentyl-2-hydroxy-4-oxo-cyclohex-2-ene-1-carboxylate
??2,4-?????-6-???????
3,5-Dibenzyloxybenzyl alcohol
??????????
3,5-???????????
3,5-Dihydroxybenzoic acid
3,5-DIMETHOXYBENZOYL???
?? ??
Olivetol ?? ??
???( 445)?? ??
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