(3,5-dimethoxyphenyl)methanol

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Names

[ CAS No. ]:
24131-31-5

[ Name ]:
(3,5-dimethoxyphenyl)methanol

[Synonym ]:
3,5-BENZYLOXYBENZYL ALCOHOL
3,5-Dibenzylooxybenzyl alcohol
[3-Benzyl-5-(benzyloxy)phenyl]methanol
RARECHEM AL BD 0734
3,5-Dibenzyloxybenzyl alkohol
3,5-Bis(benzyloxy)benzyl Alcohol
Benzenemethanol, 3-(phenylmethoxy)-5-(phenylmethyl)-
MFCD01863236
(3,5-dimethoxyphenyl)methanol

Chemical & Physical Properties

[ Density]:
1.1±0.1 g/cm3

[ Boiling Point ]:
480.2±40.0 °C at 760 mmHg

[ Melting Point ]:
78-81 °C(lit.)

[ Molecular Formula ]:
C21H20O2

[ Molecular Weight ]:
304.382

[ Flash Point ]:
219.6±21.6 °C

[ Exact Mass ]:
304.146332

[ PSA ]:
38.69000

[ LogP ]:
4.59

[ Vapour Pressure ]:
0.0±1.3 mmHg at 25°C

[ Index of Refraction ]:
1.614

MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Hazard Codes ]:
Xn

[ Safety Phrases ]:
S24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2909499000

Synthetic Route

Precursor & DownStream

Precursor

  • Benzoic acid,3,5-bis(phenylmethoxy)-, methyl ester
  • benzyl 3,5-bis(phenylmethoxy)benzoate
  • 3,5-Dihydroxybenzyl alcohol
  • Benzyl chloride
  • Benzyl bromide
  • Methyl 3,5-dihydroxybenzoate
  • 3,5-Dihydroxybenzoic acid
  • ethyl 3,5-bis(phenylmethoxy)benzoate
  • 3,5-DIBENZYLOXYBENZOIC ACID

DownStream

  • 1,3-Dibenzyloxybenzene
  • Olivetol
  • Isorhapotogenin
  • Rhapontigenin
  • Resveratrol
  • methyl 3,5-dibenzyloxybenzoate
  • 3,5-Dihydroxybenzyl alcohol
  • [3,5-bis[[3,5-bis(phenylmethoxy)phenyl]methoxy]phenyl]methanol
  • 5-(bromomethyl)benzene-1,3-diol
  • 3,5-BIS[3,5-BIS(BENZYLOXY)BENZYLOXY]BENZYL BROMIDE

Customs

[ HS Code ]: 2909499000

[ Summary ]:
2909499000. ether-alcohols and their halogenated, sulphonated, nitrated or nitrosated derivatives. VAT:17.0%. Tax rebate rate:9.0%. . MFN tariff:5.5%. General tariff:30.0%

Articles

9-Membered carbocycle formation: development of distinct Friedel-Crafts cyclizations and application to a scalable total synthesis of (±)-caraphenol A.

Angew. Chem. Int. Ed. Engl. 53(13) , 3409-13, (2014)

Explorations into a series of different approaches for 9-membered carbocycle formation have afforded the first reported example of a 9-exo-dig ring closure via a Au(III)-promoted reaction between an a...

B(C6F5)3: an efficient catalyst for reductive alkylation of alkoxy benzenes and for synthesis of triarylmethanes using aldehydes. Chandrasekhar S, et al.

Tetrahedron Lett. 50(48) , 6693-6697, (2009)

The structure and partial synthesis of imbricatine, a benzyltetrahydroisoquinoline alkaloid from the starfish Dermasterias imbricata. Burgoyne DL, et al.

Can. J. Chem. 69(1) , 20-27, (1991)


More Articles


Related Compounds

  • (3,5-Dimethoxyphenyl)methanol
  • bis(3,5-dimethoxyphenyl)methanol
  • benzoic acid,(3,5-dimethoxyphenyl)methanol
  • (3,5-DIMETHOXYPHENYL)METHANOL-4-BORONIC ACID
  • (BENZODIOXOL-5-YL)(3,5-DIMETHOXYPHENYL)METHANOL
  • (E)-2,4-dimethoxy-6-(4-methoxystyryl)phenyl-(3,5-dimethoxyphenyl)methanol
  • 2-(5,5-Dimethyl-2,4-dioxoimidazolidin-1-yl)acetonitrile
  • 2-(2-Aminoethanesulfonyl)-2-methylpropane hydrochloride
  • N-[2-(methylamino)ethyl]methanesulfonamide hydrochloride
  • 1-(1,3-Thiazol-2-yl)piperidine-4-carboxylic acid hydrochloride
  • 4-(4-Ethylpiperazin-1-yl)-3-fluorobenzoic acid hydrochloride
  • 2-[3-(Aminomethyl)phenoxy]butanenitrile hydrochloride
  • 1-(3-Aminopropoxy)-1,2,3,4-tetrahydronaphthalene hydrochloride
  • 1-[2-(4-Methoxyphenyl)-4-methyl-1,3-thiazol-5-yl]ethan-1-amine hydrochloride
  • 2-(2-Chloro-4-fluorophenyl)propan-2-amine
  • propan-2-yl (2S)-2-amino-4-methylpentanoate hydrochloride
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