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Benzenemethanol, α-ethyl-2,3,6-trimethoxy-, also known as 2,3,6-trimethoxy-α-ethylbenzenemethanol, is an organic compound with the chemical formula C11H16O3. It is a derivative of benzyl alcohol, featuring a benzene ring with a hydroxyl group attached to the carbon atom, an ethyl group at the α-position, and three methoxy groups at the 2, 3, and 6 positions. Benzenemethanol, a-ethyl-2,3,6-trimethoxy- is characterized by its aromatic structure and the presence of multiple functional groups, which contribute to its unique chemical properties and potential applications in various fields, such as pharmaceuticals and chemical synthesis.

5556-78-5

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5556-78-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5556-78-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,5 and 6 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5556-78:
(6*5)+(5*5)+(4*5)+(3*6)+(2*7)+(1*8)=115
115 % 10 = 5
So 5556-78-5 is a valid CAS Registry Number.

5556-78-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2,3,6-trimethoxyphenyl)-1-propanol

1.2 Other means of identification

Product number -
Other names Ethyl-2,3,6-trimethoxyphenylcarbinol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5556-78-5 SDS

5556-78-5Relevant academic research and scientific papers

Synthesis, antiepileptic effects, and structure-activity relationships of α-asarone derivatives: In vitro and in vivo neuroprotective effect of selected derivatives

Zhang, Jian,Mu, Keman,Yang, Peng,Feng, Xinqian,Zhang, Di,Fan, Xiangyu,Wang, Qiantao,Mao, Shengjun

, (2021/08/03)

In the present study, we compared the antiepileptic effects of α-asarone derivatives to explore their structure-activity relationships using the PTZ-induced seizure model. Our research revealed that electron-donating methoxy groups in the 3,4,5-position on phenyl ring increased antiepileptic potency but the placement of other groups at different positions decreased activity. Besides, in allyl moiety, the optimal activity was reached with either an allyl or a 1-butenyl group in conjugation with the benzene ring. The compounds 5 and 19 exerted better neuroprotective effects against epilepsy in vitro (cell) and in vivo (mouse) models. This study provides valuable data for further exploration and application of these compounds as potential anti-seizure medicines.

Feeding-deterrent activity of α-asarone isomers against some stored Coleoptera

Poplewski, Janusz,Lozowicka, Bozena,Dubis, Alina T.,Lachowska, Barbara,Winiecki, Zbigiew,Nawrot, Jan

, p. 560 - 564 (2007/10/03)

All isomers of α-asarone [(E)-4-prop-1-enyl-1,2,5-trimethoxybenzene] were tested for their feeding deterrent activity against adults of Sitophilus granarius and Tribolium confusum and larvae of Trogoderma granarium and Tribolium confusum. (E)-2-prop-1-eny

Synthesis and hypolipidemic and antiplatelet activities of α-asarone isomers in humans (in vitro), mice (in vivo), and rats (in vivo)

Poplawski,Lozowicka,Dubis,Lachowska,Witkowski,Siluk,Petrusewicz,Kaliszan,Cybulski,Strzalkowska,Chilmonczyk

, p. 3671 - 3676 (2007/10/03)

A series of α-asarone isomers was synthesized and investigated for their hypolipidemic and antiplatelet activity. Considering the hypolipidemic activity in rats at a dose of 80 mg/kg/day, some isomers were more potent than clofibrate at 150 mg/kg. Compoun

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