3,5-Dimethoxybenzyl chloride

Names

[ CAS No. ]:
6652-32-0

[ Name ]:
3,5-Dimethoxybenzyl chloride

[Synonym ]:
MFCD00074902
1-(chloromethyl)-3,5-dimethoxybenzene

Chemical & Physical Properties

[ Density]:
1.13 g/cm3

[ Boiling Point ]:
115-118 °C0.4 mm Hg(lit.)

[ Melting Point ]:
46-48 °C(lit.)

[ Molecular Formula ]:
C₉H₁₁ClO₂

[ Molecular Weight ]:
186.63500

[ Flash Point ]:
>230 °F

[ Exact Mass ]:
186.04500

[ PSA ]:
18.46000

[ LogP ]:
2.44260

MSDS

Safety Information

[ Symbol ]:

GHS05, GHS07

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H314-H335

[ Precautionary Statements ]:
P261-P280-P305 + P351 + P338-P310

[ Personal Protective Equipment ]:
Eyeshields;Faceshields;full-face particle respirator type N100 (US);Gloves;respirator cartridge type N100 (US);type P1 (EN143) respirator filter;type P3 (EN 143) respirator cartridges

[ Hazard Codes ]:
C: Corrosive;

[ Risk Phrases ]:
R34;R36/37

[ Safety Phrases ]:
S26-S27-S28-S36/37/39-S45

[ RIDADR ]:
UN 3261 8/PG 2

[ WGK Germany ]:
3

[ Packaging Group ]:
III

[ Hazard Class ]:
8

[ HS Code ]:
2909309090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

3,5-Dimethoxybenzylalcohol
Methyl 3,5-dimethoxybenzoate
3,5-Dimethoxybenzaldehyde
3,5-Dimethoxybenzoic acid
3,5-Dihydroxybenzoic acid
ethyl 3,5-dimethoxybenzoate

DownStream

2-bromo-1-(chloromethyl)-3,5-dimethoxybenzene
pterostilbene
(Z)-PTEROSTILBENE
4,5-Dimethylresorcinol
resveratrol triacetate
Resveratrol
diethyl 3,5-dimethoxybenzylphosphonate
3,3',5,5'-Tetramethoxy-bibenzyl
Benzenemethanamine,2,4-dimethoxy-N,N,6-trimethyl-

Customs

[ HS Code ]: 2909309090

[ Summary ]:
2909309090 other aromatic ethers and their halogenated, sulphonated, nitrated or nitrosated derivatives VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0%

Articles

Synthesis and anti-inflammatory activity of resveratrol analogs.

Chem. Pharm. Bull. 53(!2) , 1587-90, (2005)

Seventeen novel resveratrol derivatives were synthesized. Their anti-inflammatory activities were tested on xylene-induced mouse ear edema. The pharmacological results showed that some compounds have ...

Synthesis of (±)-dimethyl curvularin based on the palladium-catalyzed carbonylation of 3, 5-dimethoxybenzyl chloride using a butadiene telomer as a building block. Takahashi T, et al.

Tetrahedron Lett. 21(40) , 3885-88, (1980)

3,5-dimethoxybenzyl chloride
2-bromo-3,5-dimethoxybenzyl chloride
(3,5-Dimethoxybenzyl)methylamine
(3,5-DIMETHOXYBENZYL)TRIPHENYLPHOSPHONIUM BROMIDE
3,5-dimethoxybenzyl 3,5-bis(trifluoromethyl)phenyl sulfone
3,5-dimethoxybenzyl iodide
Tert-butyl 6'-bromo-1',2'-dihydrospiro[cyclopentane-1,3'-indole]-1'-carboxylate
benzyl N-[methyl({8-oxa-1-azaspiro[4.5]decan-3-yl})oxo-lambda6-sulfanylidene]carbamate
tert-butyl N-(5-bromo-1-methyl-2,6-dioxo-3-propyl-1,2,3,6-tetrahydropyrimidin-4-yl)carbamate
benzyl N-[(4-bromo-2,6-dimethylphenyl)methyl]-N-methylcarbamate
4-[(cyclopropylamino)methyl]-1-ethyl-1H-pyrazole-5-sulfonamide
Benzyl 2-(3-bromo-2-methylphenyl)pyrrolidine-1-carboxylate
Butyl 3-(5-chloro-1,2,4-thiadiazol-3-yl)-2-acetamidopropanoate
trans-1-Benzyl-2-phenyl-pyrrolidin-3-OL
7-[4-Nitro-2-(trifluoromethyl)phenoxy][1,2,4]triazolo[1,5-a]pyridine
Tert-butyl 3-hydroxy-3-(2-phenylethyl)piperidine-1-carboxylate

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