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346656-34-6

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  • SAGECHEM/ 2-(2-Carbethoxyphenyl)-5,5-Dimethyl-1,3,2-Dioxaborinane /Manufacturer in China

    Cas No: 346656-34-6

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346656-34-6 Usage

Uses

Different sources of media describe the Uses of 346656-34-6 differently. You can refer to the following data:
1. A boronic acid ester derivative as inhibitor of hormone-sensitive lipase
2. A boronic acid ester derivative as inhibitor of hormone-sensitive lipase.

Check Digit Verification of cas no

The CAS Registry Mumber 346656-34-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,6,6,5 and 6 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 346656-34:
(8*3)+(7*4)+(6*6)+(5*6)+(4*5)+(3*6)+(2*3)+(1*4)=166
166 % 10 = 6
So 346656-34-6 is a valid CAS Registry Number.
InChI:InChI=1/C14H19BO4/c1-4-17-13(16)11-7-5-6-8-12(11)15-18-9-14(2,3)10-19-15/h5-8H,4,9-10H2,1-3H3

346656-34-6 Well-known Company Product Price

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  • TCI America

  • (E0667)  Ethyl 2-(5,5-Dimethyl-1,3,2-dioxaborinan-2-yl)benzoate  >98.0%(T)

  • 346656-34-6

  • 1g

  • 1,190.00CNY

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346656-34-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)benzoate

1.2 Other means of identification

Product number -
Other names 2-(5,5-Dimethyl-1,3,2-dioxaborinan-2-yl)benzoic Acid Ethyl Ester

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:346656-34-6 SDS

346656-34-6Relevant articles and documents

Indeno[1,2-b]fluorene-Based [2,2]Cyclophanes with 4n/4n and 4n/[4n+2] π Electrons: Syntheses, Structural Analyses, and Excitonic Coupling Properties

Wang, Chi-Shin,Wei, Yu-Chen,Chang, Kai-Hsin,Chou, Pi-Tai,Wu, Yao-Ting

, p. 10158 - 10162 (2019)

Indeno[1,2-b]fluorene-based [2,2]cyclophanes with 4n/4n and 4n/[4n+2] π-electron systems were prepared, and their structures were identified by X-ray crystallography. With short π–π distances around 3.0 ?, [2.2](5,11)indeno[1,2-b]fluorenophane and its pre

Synthesis of substituted diazino[c]quinolin-5(6H)-ones, diazino[c]isoquinolin-6(5H)-ones, diazino[c]naphthyridin-6(5H)-ones and diazino[c]naphthyridin-5(6H)-ones

Fresneau, Nathalie,Cailly, Thomas,Fabis, Frédéric,Bouillon, Jean-Philippe

, p. 5393 - 5400 (2013/07/05)

Substituted diazino[c]quinolin-5(6H)-ones and -isoquinolin-6(5H)-ones, diazino[c]naphthyridin-6(5H)- and -5(6H)-ones were obtained using two synthetic routes: one-pot cross-coupling/cyclisation and two-step cross-coupling/KOH- mediated anionic ring closur

Synthesis of Ortho Substituted Arylboronic Esters by in Situ Trapping of Unstable Lithio Intermediates

Kristensen, Jesper,Lysen, Morten,Vedso, Per,Begtrup, Mikael

, p. 1435 - 1437 (2007/10/03)

matrix presented Ortho lithiation-in situ boration using lithium 2,2,6,6-tetramethylpiperidide (LTMP) in combination with triisopropylborate (B(OiPr)3) is a highly efficient and experimentally straightforward process for the preparation of ortho substituted arylboronic esters. The mild reaction conditions allow the presence of functionalities such as ester or cyano groups or halogen substituents that are usually not compatible with the conditions used in directed ortho metalation of arenes. The arylboronic esters underwent Suzuki-type cross-coupling with a range of aryl halides, furnishing biaryls in 53-94% yield.

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