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380430-67-1

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380430-67-1 Usage

General Description

(2,3,6-TRIMETHOXY)BENZENEBORONIC ACID is a chemical compound with the molecular formula C9H13BO5. It is a boronic acid derivative that contains three methoxy groups attached to the benzene ring. (2,3,6-TRIMETHOXY)BENZENEBORONIC ACID is valuable in organic synthesis as a reagent for the Suzuki-Miyaura coupling reaction, which is a widely used method for the formation of carbon-carbon bonds. (2,3,6-TRIMETHOXY)BENZENEBORONIC ACID is used in the preparation of various biologically active compounds and pharmaceuticals. It is also used in the development of materials for advanced electronic and optoelectronic devices. Additionally, it has potential applications in the field of medicinal chemistry and drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 380430-67-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,0,4,3 and 0 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 380430-67:
(8*3)+(7*8)+(6*0)+(5*4)+(4*3)+(3*0)+(2*6)+(1*7)=131
131 % 10 = 1
So 380430-67-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H13BO5/c1-13-6-4-5-7(14-2)9(15-3)8(6)10(11)12/h4-5,11-12H,1-3H3

380430-67-1 Well-known Company Product Price

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  • Alfa Aesar

  • (H53197)  2,3,6-Trimethoxybenzeneboronic acid, 95%   

  • 380430-67-1

  • 250mg

  • 463.0CNY

  • Detail
  • Alfa Aesar

  • (H53197)  2,3,6-Trimethoxybenzeneboronic acid, 95%   

  • 380430-67-1

  • 1g

  • 1482.0CNY

  • Detail

380430-67-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,6-Trimethoxyphenylboronic acid

1.2 Other means of identification

Product number -
Other names 2,3,6-Trimethoxybenzeneboronic acid

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:380430-67-1 SDS

380430-67-1Relevant articles and documents

ENHANCING AUTOPHAGY OR INCREASING LONGEVITY BY ADMINISTRATION OF UROLITHINS OR PRECURSORS THEREOF

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Sheet 29, (2014/01/17)

Disclosed are methods, compounds, and compositions useful for increasing autophagy and promoting longevity. The methods, compounds, and compositions relate to urolithins and urolithin precursors and use thereof. Certain urolithins are represented by Formula I, while certain urolithin precursors are represented by Formula IV. The urolithin may be urolithin A, urolithin B, urolithin C, or urolithin D. The urolithin precursor may be ellagic acid or an ellagitannin. The methods include in vivo, ex vivo, and in vitro uses of the compounds and compositions.

Nonsteroidal selective glucocorticoid modulators: The effect of C-10 substitution on receptor selectivity and functional potency of 5-allyl-2,5-dihydro-2,2,4-trimethyl-lh-[1]benzopyrano[3,4-f]quinolines

Kym, Philip R.,Kort, Michael E.,Coghlan, Michael J.,Moore, Jimmie L.,Tang, Rui,Ratajczyk, James D.,Larson, Daniel P.,Elmore, Steven W.,Pratt, John K.,Stashko, Michael A.,Douglass Falls,Lin, Chun W.,Nakane, Masake,Miller, Loan,Tyree, Curtis M.,Miner, Jeffery N.,Jacobson, Peer B.,Wilcox, Denise M.,Nguyen, Phong,Lane, Benjamin C.

, p. 1016 - 1030 (2007/10/03)

The preparation and characterization of a series of C-10 substituted 5-allyl-2,5-dihydro-2,2,4-trimethyl-1H-[1]benzopyrano[3,4-f]quinolines as a novel class of selective ligands for the glucocorticoid receptor is described. Substitution at the C-10 positi

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