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1-(3-nitropropyl)-4-octylbenzene is a chemical compound with the molecular formula C16H23NO2, characterized as a nitroalkane compound that features a nitro group and an alkyl chain attached to a benzene ring. It is a yellowish to brownish liquid with a strong odor, insoluble in water, but soluble in most organic solvents. Due to its potential risks to human health and the environment, it requires careful handling and disposal.

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  • 374077-87-9 Structure
  • Basic information

    1. Product Name: 1-(3-nitropropyl)-4-octylbenzene
    2. Synonyms: 1-(3-nitropropyl)-4-octylbenzene
    3. CAS NO:374077-87-9
    4. Molecular Formula:
    5. Molecular Weight: 277.407
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 374077-87-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1-(3-nitropropyl)-4-octylbenzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(3-nitropropyl)-4-octylbenzene(374077-87-9)
    11. EPA Substance Registry System: 1-(3-nitropropyl)-4-octylbenzene(374077-87-9)
  • 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: 374077-87-9(Hazardous Substances Data)

374077-87-9 Usage

Uses

Used in Industrial Production:
1-(3-nitropropyl)-4-octylbenzene is used as a chemical intermediate for the production of various industrial products and pharmaceuticals, leveraging its unique chemical structure and properties.
Used in Pharmaceutical Industry:
1-(3-nitropropyl)-4-octylbenzene is used as a building block for the synthesis of certain pharmaceutical compounds, contributing to the development of new drugs and therapies.
Used in Chemical Research:
1-(3-nitropropyl)-4-octylbenzene is also utilized in chemical research as a model or reference substance for studying the properties and reactivity of nitroalkane compounds and their potential applications in various chemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 374077-87-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,7,4,0,7 and 7 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 374077-87:
(8*3)+(7*7)+(6*4)+(5*0)+(4*7)+(3*7)+(2*8)+(1*7)=169
169 % 10 = 9
So 374077-87-9 is a valid CAS Registry Number.

374077-87-9Relevant articles and documents

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.

A hydrochloric acid profuse spear Pidotimod synthetic method and intermediate

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, (2017/04/27)

The invention provides a method and an intermediate for synthesizing Fingolimod hydrochloride. The method comprises the following steps: performing nitro-substitution, formaldehyde condensation, reduction and salification on octyl halogenated propylbenzene by using a novel intermediate, thereby obtaining the Fingolimod hydrochloride. The synthetic method is short in route, high in yield, low in cost, mild in reaction conditions, simple and convenient in operation and high in product purity and has high application value in large-scale industrial production.

PREPARATION OF FINGOLIMOD AND ITS SALTS

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, (2014/09/03)

The present application provide processes for the preparation of fingolimod and its pharmaceutically acceptable salts, process for the purification of fingolimod hydrochloride and process for the preparation of amorphous fingolimod hydrochloride.

METHODS AND COMPOUNDS FOR THE PREPARATION OF FLUORINE-LABELED DEOXY-FTY720

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Page/Page column 18-19, (2012/01/06)

Highly efficient processes for making radioactive and non-radioactive Fluorodeoxy- FTY720 are provided. Also provided are novel precursor compounds included in such processes. In addition the present invention prov ides compounds useful in the treatment a

Synthesis of 2-nitroalcohols by regioselective ring opening of epoxides with MgSO4/MeOH/NaNO2 system: A short synthesis of immunosuppressive agent FTY-720

Kalita,Barua,Bezbarua,Bez

, p. 1411 - 1414 (2007/10/03)

It has been demonstrated that a variety of epoxides can easily be opened with a system consisting of MgSO4/MeOH/NaNO2 giving the corresponding 2-nitroalcohols in excellent yields. This strategy has been applied to achieve a short synthesis of Immunosuppressive Agent FTY - 720.

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