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198623-56-2

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198623-56-2 Usage

General Description

3,5-Diethoxybenzyl alcohol is a chemical compound that belongs to the category of benzyl alcohols. It is a white solid with a molecular formula C12H18O3 and a molecular weight of 210.27 g/mol. 3,5-Diethoxybenzyl alcohol is commonly used as a reagent in organic synthesis and pharmaceutical research due to its potential as a building block for various chemical reactions. Its properties make it a valuable intermediate in the production of pharmaceuticals, agrochemicals, and other fine chemicals. In addition, 3,5-Diethoxybenzyl alcohol is also used in the manufacturing of fragrances, dyes, and pigments. However, it is important to handle this compound with care, as it may cause irritation to the skin, eyes, and respiratory system, and should be stored and used in a well-ventilated area.

Check Digit Verification of cas no

The CAS Registry Mumber 198623-56-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,8,6,2 and 3 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 198623-56:
(8*1)+(7*9)+(6*8)+(5*6)+(4*2)+(3*3)+(2*5)+(1*6)=182
182 % 10 = 2
So 198623-56-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H16O3/c1-3-13-10-5-9(8-12)6-11(7-10)14-4-2/h5-7,12H,3-4,8H2,1-2H3

198623-56-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (3,5-Diethoxyphenyl)methanol

1.2 Other means of identification

Product number -
Other names 3,5-Diethoxybenzyl alcohol

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:198623-56-2 SDS

198623-56-2Relevant articles and documents

Total synthesis of dysidavarone A

Yu, Chunhui,Zhang, Xiaoguang,Zhang, Jinghua,Shen, Zhengwu

, p. 4337 - 4345 (2016)

Dysidavarone A is a sesquiterpene isolated from the South China Sea sponge Dysidea avara and was reported that it showed significant anticancer activities. Because the compound has unique ‘dysidavarane’ carbon skeleton and potent biological activity, a se

Synthesis and potent antileukemic activities of 10-benzyl-9(10H)-acridinones

Gao, Chunmei,Jiang, Yuyang,Tan, Chunyan,Zu, Xuyu,Liu, Huachen,Cao, Derong

, p. 8670 - 8675 (2008/12/23)

A novel series of 10-benzyl-9(10H)-acridinones and 1-benzyl-4-piperidones were synthesized and tested for their in vitro antitumor activities against CCRF-CEM cells. Assay-based antiproliferative activity study using CCRF-CEM cell lines revealed that the acridone group and the substitution pattern on the benzene unit had significant effect on cytotoxicity of this series of compounds, among which 10-(3,5-dimethoxy)benzyl-9(10H)-acridinone (3b) was found to be the most active compound with IC50 at about 0.7 μM. Compound 3b was also found to have antiproliferative activity against two other human leukemic cell lines K562 and HL60 using the MTT assay. The antitumor effect of 3b is believed to be due to the induction of apoptosis, which is further confirmed by PI (Propidium iodide) staining and Annexin V-FITC/PI staining assay using flow cytometry analysis.

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