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51829-43-7

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51829-43-7 Usage

Explanation

The molecular formula represents the number of carbon (C), hydrogen (H), and oxygen (O) atoms in a molecule of 1,4-Benzenedimethanol, 2,5-dimethoxy-.

Explanation

1,4-Benzenedimethanol, 2,5-dimethoxyis derived from benzene, a basic aromatic hydrocarbon with a six-carbon ring structure.

Explanation

The compound contains two hydroxyl (-OH) groups, which are functional groups consisting of an oxygen atom bonded to a hydrogen atom.

Explanation

The compound also contains two methoxy (-OCH3) groups, which are functional groups consisting of an oxygen atom bonded to a methyl group (CH3).

Explanation

1,4-Benzenedimethanol, 2,5-dimethoxyis utilized in the synthesis of various pharmaceuticals, contributing to the development of new drugs and medications.

Explanation

The compound serves as a building block for the production of other organic compounds, making it a versatile chemical intermediate.

Explanation

1,4-Benzenedimethanol, 2,5-dimethoxypossesses distinct chemical properties that make it valuable in scientific research and laboratory settings.

Explanation

If not properly handled and stored, 1,4-Benzenedimethanol, 2,5-dimethoxymay pose health risks to individuals who come into contact with it.

Explanation

It is crucial to handle and store 1,4-Benzenedimethanol, 2,5-dimethoxywith care to minimize the risk of exposure and ensure the safety of those working with the compound.

Derivative of benzene

Yes

Hydroxyl groups

Two

Methoxy groups

Two

Pharmaceutical synthesis

Used in

Building block for organic compounds

Yes

Unique chemical properties

Known for

Health risks

Potential

Handling and storage

Caution required

Check Digit Verification of cas no

The CAS Registry Mumber 51829-43-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,8,2 and 9 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 51829-43:
(7*5)+(6*1)+(5*8)+(4*2)+(3*9)+(2*4)+(1*3)=127
127 % 10 = 7
So 51829-43-7 is a valid CAS Registry Number.

51829-43-7Relevant articles and documents

Faurine and O-methylfaurine, two novel benzyl-aporphine dimers from Thalictrum fauriei

Lee, Shoei-Sheng,Doskotch, Raymond W.

, p. 738 - 743 (1996)

Two new benzyl-aporphine dimers, faurine (1) and its O-methyl ether (2), were obtained from Thalictrum fauriei and their structures determined by spectral and chemical methods. Faurine (1), the first dimer with the diphenyl ether connection at C-1 of the aporphine, did not undergo a Hofmann degradation, yet formed a chiral phenanthrene product (6) with cyanogen bromide. Two nondimeric chiral aporphine alkaloids, O-acetylisocorydine and O-methylisocorydine, gave the corresponding phenanthrene products 7 and 8, respectively, under the same conditions, but only compound 7 was optically active.

ELECTROCHEMICALLY ACTIVE AGENTS FOR PH MODULATION IN BIOLOGICAL BUFFERS

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Paragraph 00304, (2017/01/26)

Device and methods for use in a biosensor comprising a multisite array of test sites, the device and methods being useful for modulating the binding interactions between a (biomolecular) probe or detection agent and an analyte of interest by modulating the pH or ionic gradient near the electrodes in such biosensor. An electrochemically active agent comprising quinone derivatives that is suitable for use in biological buffers for changing the pH of the biological buffers. Method for changing the pH of biological buffers using the electrochemically active agents. The methods of modulating the binding interactions provided in a biosensor, analytic methods for more accurately controlling and measuring the pH or ionic gradient near the electrodes in such biosensor, and analytic methods for more accurately measuring an analyte of interest in a biological sample.

Mono and bis(bioreductive) alkylating agents: Synthesis and antitumor activities in a B16 melanoma model

Witiak,Loper,Ananthan,Almerico,Verhoef,Filppi

, p. 1636 - 1642 (2007/10/02)

Several potentially bis(alkylating) bis(quinones) (3-5) and 1,4- and 1,3-bis(alkylating) monoquinones (6-13) belonging to general structure 2,2'-ethylenebis[5-[(leaving group) methyl]-1,4-benzoquinone] (3-5) and 2,5- and 2,6-bis[(leaving group)methyl]-1,4

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