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(3,5-dimethoxyphenyl)methanol

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

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

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