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70654-71-6

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70654-71-6 Usage

General Description

4-bromo-2,6-dimethoxyphenol is a chemical compound with the molecular formula C8H9BrO3. It is an aromatic organic compound that contains a bromine atom and two methoxy groups attached to a phenol ring. 4-bromo-2,6-dimethoxyphenol has been studied for its potential pharmaceutical properties, including its antioxidant and antimicrobial activities. It is also used in the synthesis of other organic compounds, and as a building block in medicinal chemistry. Additionally, 4-bromo-2,6-dimethoxyphenol has been investigated for its potential use in industrial applications, such as in the development of new materials and as a chemical intermediate in the production of other compounds. Overall, this chemical compound is of interest for its potential biological and industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 70654-71-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,6,5 and 4 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 70654-71:
(7*7)+(6*0)+(5*6)+(4*5)+(3*4)+(2*7)+(1*1)=126
126 % 10 = 6
So 70654-71-6 is a valid CAS Registry Number.

70654-71-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-bromo-2,6-dimethoxyphenol

1.2 Other means of identification

Product number -
Other names 4-bromosyringol

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:70654-71-6 SDS

70654-71-6Relevant articles and documents

Aqueous Assembly of Zwitterionic Daisy Chains

Aeschi, Yves,Drayss-Orth, Sylvie,Valá?ek, Michal,H?ussinger, Daniel,Mayor, Marcel

, p. 285 - 295 (2019)

The synthesis and characterization of zwitterionic molecular [c2]- and [a2]-daisy chains are described, relying on recognition of a positively charged cyclophane and a negatively charged oligo(phenylene-ethynylene) (OPE) rod in aqueous medium. For this pu

BRD9 BIFUNCTIONAL DEGRADERS AND THEIR METHODS OF USE

-

Page/Page column 191, (2021/04/01)

The disclosure provides BRD9 bifunctional compounds of Formula (A) or a pharmaceutically acceptable salt, hydrate, solvate, prodrug, stereoisomer, or tautomer thereof, to their preparation, to pharmaceutical compositions comprising them, and to their use in the treatment of diseases and disorders mediated by a bromodomain-containing protein, such as bromodoma in-containing protein 9 (BRD9)

Stereoselective Total Synthesis of (+)-Aristolactam GI

Luong, Tuan M.,Pilkington, Lisa I.,Barker, David

, p. 5747 - 5756 (2019/05/10)

Aristolactams are an important subgroup of aporphinoids, which all share a common phenanthrene chromophore motif that is thought to be responsible for the range of interesting physicochemical and biological properties exhibited by these compounds. Among all of the aristolactams discovered, (+)-aristolactam GI displays a unique structural feature of having the aristolactam scaffold linked via a benzodioxane ring to a phenyl propanoid unit, resulting in the compound being an aporphinoid-lignan hybrid. The synthesis of (+)-aristolactam GI was achieved first by synthesis of an orthogonally protected aristolactam, which was prepared using a Suzuki/aldol cascade to convert a differentially protected isoindolin-1-one to the required phenanthrene. The required enantiopure phenyl propanoid unit was prepared from readily available (R)-methyl lactate. A selective Mitsunobu reaction was used to combine these two key fragments, prior to the formation of the linking benzodioxane in the final step. The absolute stereochemistry of the natural product was confirmed to be 7′S, 8′S.

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