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115377-93-0

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115377-93-0 Usage

General Description

2-(methoxymethoxy)phenylboronic acid is a boronic acid compound with the chemical formula C8H11BO4. It is commonly used as a reagent in organic synthesis and as a building block in the production of pharmaceuticals and agrochemicals. This chemical is known for its ability to form stable complexes with diols, making it useful for the selective recognition and binding of certain biomolecules. Additionally, it has been studied for its potential applications in catalysis and materials science. Overall, 2-(methoxymethoxy)phenylboronic acid is a versatile and important compound with a wide range of potential uses in various fields of chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 115377-93-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,3,7 and 7 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 115377-93:
(8*1)+(7*1)+(6*5)+(5*3)+(4*7)+(3*7)+(2*9)+(1*3)=130
130 % 10 = 0
So 115377-93-0 is a valid CAS Registry Number.

115377-93-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(Methoxymethoxy)phenylboronic acid

1.2 Other means of identification

Product number -
Other names [2-(Methoxymethoxy)phenyl]boronic 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:115377-93-0 SDS

115377-93-0Relevant articles and documents

The metal complex, and (meth) acrylic acid ester copolymer of olefin / α - using the same (by machine translation)

-

Paragraph 0067; 0068; 0071, (2019/11/05)

(Meth) acrylic acid ester of a high molecular weight copolymer [a] catalyst. The metal complex represented by the general formula [a] (A). [In the formula, R9 - R13 Hydrogen, a substituent represented by the general formula (B) (R14 And R15 The, are each independently hydrogen or a hydrocarbon group of 1 - 6 carbon atoms which may have a hetero atom, may form a ring together), 6 - 12 carbon atoms with an aryl group, an adamantyl group, OR2 , SR2 , Or N (R2 )2 , Represents. However, R9 - R13 One of the, at least one substituent represented by the general formula (B) 1, 6 - 12 carbon atoms of an aryl group, an adamantyl group, OR2 , SR2 , Or N (R2 )2 In. ]Figure 1 [drawing] (by machine translation)

Hydrogen bonds in phenylboronic acids with polyoxaalkyl substituents at ortho-position

Adamczyk-Wo?niak, Agnieszka,Cyrański, Micha? K.,Dabrowska, Aldona,Gierczyk, B?azej,Klimentowska, Paulina,Schroeder, Grzegorz,Zubrowska, Anna,Sporzyński, Andrzej

, p. 430 - 435 (2009/07/18)

Phenylboronic acids with polyoxaalkyl substituents at ortho position were synthesized from the corresponding bromides. Structures in solid state, determined by single crystal X-ray diffraction, reveal the presence of inter- and intramolecular hydrogen bonds. Presence of several oxygen atoms in oxaalkyl chains enables the formation of intramolecular hydrogen bonds by B(OH)2 group with different oxygen centers which lead to the formation of bifurcated hydrogen bonds. Investigated compounds were characterized by 1H, 13C, 11B and 17O NMR spectroscopy in solution. Assignment of 1H and 13C signals was made on the basis of HSQC and HMBC spectra. 17O NMR spectra show that in acetonitrile solution hydrogen bonds with solvent molecules are predominant.

Biphenyl derivatives substituted by an aromatic or heteroaromatic radical and pharamaceutical and cosmetic compositions containing same

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, (2008/06/13)

“Biphenyl derivatives substituted with an aromatic or heteroaromatic radical, and pharmaceutical and cosmetic compositions containing them” in which: Ar represents an aromatic or a heteroaromatic radical optionally substituted, in particular, with an alkyl or a carboxyl group, R2and R3represent, in particular, H or alkyl, or R2and R3, taken together, form a 5- or 6-membered ring, R4and R5represent, in particular, H or halogen, R6represents, in particular, H or lower alkyl, and the salts of the compounds of formula (I). These compounds can be used in particular in the treatment of dermatological complaints associated with a keratinization disorder, and for combating ageing of the skin.

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