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3-(hydroxymethyl)-3-nitro-1-(4-octylphenyl)-Ben is a complex organic chemical compound characterized by the presence of a hydroxymethyl group, a nitro group, and a benzene ring that is connected to an octylphenyl group. This unique molecular structure endows the compound with specific properties, such as solubility, reactivity, and stability, which may be advantageous in various applications across different industries.

899822-99-2

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899822-99-2 Usage

Uses

Used in Organic Synthesis:
3-(hydroxymethyl)-3-nitro-1-(4-octylphenyl)-Ben is used as a key intermediate in organic synthesis for the production of various complex organic molecules. Its unique functional groups allow for versatile chemical reactions, facilitating the synthesis of a wide range of compounds with potential applications in pharmaceuticals, materials science, and other fields.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3-(hydroxymethyl)-3-nitro-1-(4-octylphenyl)-Ben is used as a building block for the development of new drugs. Its molecular structure can be modified to create novel drug candidates with potential therapeutic effects. 3-(hydroxymethyl)-3-nitro-1-(4-octylphenyl)-Ben's reactivity and stability make it suitable for the synthesis of pharmaceutical agents that can target specific biological pathways or receptors.
Used in Materials Science:
3-(hydroxymethyl)-3-nitro-1-(4-octylphenyl)-Ben is used as a component in the development of advanced materials with unique properties. Its incorporation into polymers, coatings, or other materials can enhance their performance, such as improving their mechanical strength, thermal stability, or chemical resistance. 3-(hydroxymethyl)-3-nitro-1-(4-octylphenyl)-Ben's versatility in chemical reactions allows for the creation of materials with tailored properties for specific applications.
Further research and testing are necessary to fully explore and harness the potential of 3-(hydroxymethyl)-3-nitro-1-(4-octylphenyl)-Ben in commercial and industrial applications. Its unique molecular structure and properties offer promising opportunities for innovation and advancement in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 899822-99-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,9,8,2 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 899822-99:
(8*8)+(7*9)+(6*9)+(5*8)+(4*2)+(3*2)+(2*9)+(1*9)=262
262 % 10 = 2
So 899822-99-2 is a valid CAS Registry Number.

899822-99-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(hydroxymethyl)-3-nitro-1-(4-octylphenyl)butane-1,4-diol

1.2 Other means of identification

Product number -
Other names 3-(hydroxymethyl)-3-nitro-1-(4-octylphenyl)-Ben

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:899822-99-2 SDS

899822-99-2Relevant academic research and scientific papers

An alternative efficient approach for the synthesis of Fingolimod hydrochloride

Vinigari, Krishna,Jonnada, Krishna,Mohammed, Noorjahan,Kotu, Girija Mangatayaru

, p. 39 - 48 (2019/01/21)

An efficient process for the synthesis of API Fingolimod Hydrochloride is presented. This proposed synthesis involves simple commercially available octanophenone as a starting material. The route is effective involving seven steps to achieve the target, thus reducing the cycle time, and is cost efficient by 50%. It is an immune modulating drug for the treatment of heart failure and arrhythmias.

PROCESS FOR MAKING FINGOLIMOD

-

, (2012/04/17)

The invention relates to a process of making fingolimod of formula (1), or an acid addition salt thereof comprising a step of reacting the compound of formula (11) and/or a compound of formula (14) or an acid addition salt thereof, in a solvent with hydrogen in a presence of a hydrogenation catalyst, preferably palladium catalyst, and optionally converting fingolimod of formula (1) into an acidaddition salt, to compounds of formula (11) and (14) and their use in making fingolimod.

PROCESS FOR MAKING FINGOLIMOD

-

, (2012/04/17)

The invention relates to a process of making fingolimod of formula (1), or an acid addition salt thereof comprising a step of reacting the compound of formula (11) and/or a compound of formula (14) or an acid addition salt thereof, in a solvent with hydrogen in a presence of a hydrogenation catalyst, preferably palladium catalyst, and optionally converting fingolimod of formula (1) into an acid addition salt, to compounds of formula (11) and (14), processes of making them and to their use in making fingolimod.

PROCESS FOR MAKING FINGOLIMOD

-

, (2012/04/17)

The invention relates to a process of making fingolimod of formula (1), or an acid addition salt thereof comprising a step of reacting the compound of formula (11) and/or a compound of formula (14) or an acid addition salt thereof, in a solvent with hydrogen in a presence of a hydrogenation catalyst, preferably palladium catalyst, and optionally converting fingolimod of formula (1) into an acid addition salt, to compounds of formula (11) and (14), processes of making them and to their use in making fingolimod.

INTERMEDIATE COMPOUNDS AND PROCESS FOR THE PREPARATION OF FINGOLIMOD

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, (2012/05/19)

The present invention relates to processes for the preparation of (2-Amino-2-[2-(4-octylphenyl)ethyl]propane-1,3-diol hydrochloride (Fingolimod) and pharmaceutically acceptable salts thereof, and intermediates formed in such processes.

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