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Benzenemethanol, 4-(acetyloxy)-3,5-dimethoxy-, acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

18221-28-8

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18221-28-8 Usage

Chemical compound

Benzenemethanol, 4-(acetyloxy)-3,5-dimethoxy-, acetate

Category

Acetates

Derived from

Combination of benzenemethanol, 4-(acetyloxy)-3,5-dimethoxy, and acetic acid

Usage

Reagent in chemical reactions and synthesis processes

Applications

Pharmaceuticals, agrochemicals, materials sciences

Properties

Functionality: Contains acetyl and methoxy groups
Solubility: Soluble in organic solvents
Stability: Stable under proper storage conditions
Reactivity: Reactive in certain chemical reactions

Importance of handling

Care: Handle with care
Safety guidelines: Follow safety guidelines for handling and storage.

Check Digit Verification of cas no

The CAS Registry Mumber 18221-28-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,2,2 and 1 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 18221-28:
(7*1)+(6*8)+(5*2)+(4*2)+(3*1)+(2*2)+(1*8)=88
88 % 10 = 8
So 18221-28-8 is a valid CAS Registry Number.

18221-28-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name acetic acid,[4-(hydroxymethyl)-2,6-dimethoxyphenyl] acetate

1.2 Other means of identification

Product number -
Other names 3,5-dimethoxy-4-acetoxybenzyl acetate

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:18221-28-8 SDS

18221-28-8Relevant academic research and scientific papers

THREE DIHYDROISOCOUMARIN GLUCOSIDES FROM HYDRANGEA MACROPHYLLA SUBSP. SERRATA

Hashimoto, Toshihiro,Tori, Motoo,Asakawa, Yoshinori

, p. 3323 - 3330 (2007/10/02)

Three new dihydroisocoumarin glucosides, macrophyllosides A, B and C were obtained from dry leaves of Hydrangea macrophylla subsp. serrata, together with the previously known hydrangenol 8-β-glucoside.Using NMR and CD techniques and some chemical transformation, the structures were elucidated as (3S)-3',4',5'-trimethoxyphenyl-8-β-D-glucopyranosyl dihydroisocoumarin, (3R)- and (3S)-3',5'-dimethoxy-4'-hydroxyphenyl-8-β-D-glucopyranosyl dihydroisocoumarins.CD experiments indicated that hydrangenol 8-β-glucoside was the mixture of 3S- and 3R-stereoisomers.Key Word Index - Hydrangea macrophylla subsp. serrata; Saxifragaceae; macrophyllosides A, B and C; dihydroisocoumarin glucosides; bitter principles; plant growth inhibitory activity.

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