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Merck
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文件

330264

Sigma-Aldrich

3,5-二甲氧基氯苄

99%

别名:

1-(氯甲基)-3,5-二甲氧基苯

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About This Item

线性分子式:
(CH3O)2C6H3CH2Cl
CAS号:
6652-32-0
分子量:
186.64
MDL號碼:
MFCD00074902
分類程式碼代碼:
12352100
PubChem物質ID:
24859845
NACRES:
NA.22

化驗

99%

bp

115-118 °C/0.4 mmHg (lit.)

mp

46-48 °C (lit.)

SMILES 字串

COc1cc(CCl)cc(OC)c1

InChI

1S/C9H11ClO2/c1-11-8-3-7(6-10)4-9(5-8)12-2/h3-5H,6H2,1-2H3

InChI 密鑰

CCAWDIFJOBKBSE-UHFFFAOYSA-N

應用

3,5-Dimethoxybenzyl chloride was used in preparation of benzyl 7-(3,5-dimethoxyphenylacetoxy)octanoate, a precursor of curvularin. It was also used in the preparation of diethyl (3,5-dimethoxybenzyl) phosphonate via Wittig-Horner reaction.

象形圖

CorrosionExclamation mark
GHS05,GHS07

訊號詞

Danger

危險聲明

H314,H335

危險分類

Eye Dam. 1 - Skin Corr. 1B - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

8A - Combustible corrosive hazardous materials

水污染物質分類（WGK）

WGK 3

閃點（°F）

235.4 °F - closed cup

閃點（°C）

113 °C - closed cup

個人防護裝備

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

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3-甲氧基氯苄 97%

Sigma-Aldrich

209384

3-甲氧基氯苄

3,4-二甲氧基苯甲醇 96%

Sigma-Aldrich

D133000

3,4-二甲氧基苯甲醇

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 Letters, 21(40), 3885-3888 (1980)
Guoliang Chen et al.
Chemical & pharmaceutical bulletin, 53(12), 1587-1590 (2005-12-06)
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 potent anti-inflammatory activities.

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