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CAS

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216443-40-2

3-(Methoxymethoxy)phenylboronic acid, also known as "3-(Methoxymethoxy)benzeneboronic Acid", is an organic compound that falls under the category of organoboron compounds and phenylboronic acids. Its systematic name is 3-Boronobenzyl alcohol, α-((methoxy)methoxy)-, and it can be identified by its CAS Number: 443797-96-4. This chemical typically exists in a solid state and is generally used in chemical reactions as a reagent or catalyst.

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  • 216443-40-2 Structure

  • Basic information

    1. Product Name: 3-(Methoxymethoxy)phenylboronic acid
    2. Synonyms: 3-(Methoxymethoxy)phenylboronic acid
    3. CAS NO:216443-40-2
    4. Molecular Formula: C8H11BO4
    5. Molecular Weight: 181.98
    6. EINECS: N/A
    7. Product Categories: Aryl;Organoborons
    8. Mol File: 216443-40-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 357.1±52.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.19±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. PKA: 7.95±0.10(Predicted)
    10. CAS DataBase Reference: 3-(Methoxymethoxy)phenylboronic acid(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3-(Methoxymethoxy)phenylboronic acid(216443-40-2)
    12. EPA Substance Registry System: 3-(Methoxymethoxy)phenylboronic acid(216443-40-2)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 216443-40-2(Hazardous Substances Data)

216443-40-2 Usage

Uses

Used in Organic Synthesis:
3-(Methoxymethoxy)phenylboronic acid is used as a reagent for various chemical reactions, contributing to the synthesis of complex organic molecules.
Used in Suzuki Coupling:
3-(Methoxymethoxy)phenylboronic acid is used as a key component in Suzuki coupling, a type of palladium-catalyzed cross-coupling reaction. This reaction is a powerful tool for the construction of carbon–carbon bonds in organic synthesis, allowing for the formation of new compounds with potential applications in pharmaceuticals, materials science, and other fields.

Check Digit Verification of cas no

The CAS Registry Mumber 216443-40-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,6,4,4 and 3 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 216443-40:
(8*2)+(7*1)+(6*6)+(5*4)+(4*4)+(3*3)+(2*4)+(1*0)=112
112 % 10 = 2
So 216443-40-2 is a valid CAS Registry Number.

216443-40-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [3-(methoxymethoxy)phenyl]boronic acid

1.2 Other means of identification

Product number -
Other names 3-Methoxymethoxyphenylboronic 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:216443-40-2 SDS

216443-40-2Relevant articles and documents

CINNAMYL ALCOHOL DERIVATIVE COMPOUNDS AND DRUGS CONTAINING THE COMPOUNDS AS THE ACTIVE INGREDIENT

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Page/Page column 20, (2010/02/14)

A compound represented by formula (I) (wherein all the symbols are as defined in the specification) or a salt thereof Since the compound represented by formula (I) or a salt thereof has a regulatory activity for peroxisome proliferator activated receptor,

Vitamin D analogues

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Page column 13, (2010/02/09)

The present invention relates to novel triaromatic compounds having the general formula (I): as well as to a method for preparing them and to their use in pharmaceutical compositions intended for use in human or veterinary medicine (in dermatology, in car

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.

Triaromatic compounds and pharmaceutical/cosmetic compositions comprised thereof

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, (2008/06/13)

Novel pharmaceutically/cosmetically-active triaromatic compounds have the structural formula (I): and are useful for the treatment of a wide variety of disease states, whether human or veterinary, for example dermatological, rheumatic, respiratory, cardiovascular, bone and ophthalmological disorders, as well as for the treatment of mammalian skin and hair conditions/disorders.

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