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4-nitroso-m-cresol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 615-01-0 Structure
  • Basic information

    1. Product Name: 4-nitroso-m-cresol
    2. Synonyms: 4-nitroso-m-cresol;4-Nitroso-m-methylphenol;p-Nitroso-M-cresol
    3. CAS NO:615-01-0
    4. Molecular Formula: C7H7NO2
    5. Molecular Weight: 137.13598
    6. EINECS: 210-405-6
    7. Product Categories: Aromatics, Metabolites & Impurities
    8. Mol File: 615-01-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 294.6°C at 760 mmHg
    3. Flash Point: 132°C
    4. Appearance: /
    5. Density: 1.19g/cm3
    6. Vapor Pressure: 0.000913mmHg at 25°C
    7. Refractive Index: 1.553
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 6?+-.0.18(Predicted)
    11. CAS DataBase Reference: 4-nitroso-m-cresol(CAS DataBase Reference)
    12. NIST Chemistry Reference: 4-nitroso-m-cresol(615-01-0)
    13. EPA Substance Registry System: 4-nitroso-m-cresol(615-01-0)
  • 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: 615-01-0(Hazardous Substances Data)

615-01-0 Usage

Uses

A minor product formed during the metabolism of 4-nitro-m-cresol by ridgeback prawns.

Check Digit Verification of cas no

The CAS Registry Mumber 615-01-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,1 and 5 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 615-01:
(5*6)+(4*1)+(3*5)+(2*0)+(1*1)=50
50 % 10 = 0
So 615-01-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H7NO2/c1-5-4-6(9)2-3-7(5)8-10/h2-4,9H,1H3

615-01-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methyl-4-nitrosophenol

1.2 Other means of identification

Product number -
Other names 3-methyl-4-nitroso-phenol

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:615-01-0 SDS

615-01-0Relevant articles and documents

Synthesis and characterization of azoxy based mesogenic diols

Mulani, Khudbudin B.,Ganjave, Nitin V.,Chavan, Nayaku N.

, p. 359 - 362 (2014/05/06)

Azoxy based rigid mesogenic diols have been synthesized using two steps. Phenol/cresol is used as starting material. Synthesized diols are characterized by IR, 1H and 13C NMR, and mass spectroscopic methods. Thermal properties have been determined by thermo gravimetric analysis method and crystallinity patterns have been obtained by wide angle X-ray diffractogram. Substituted phenol (methyl) is used to study the effect of substitution on physical and thermal properties of rigid azoxy mesogenic diol. The detailed characterization of azoxy based rigid diols is reported in this communication, which is highly useful for fundamental and applied research, particularly in liquid crystals and liquid crystalline polymers. The experimental results reveal that phenol based rigid mesogenic diols have high thermal stability and degree of crystallinity than methyl substituted rigid mesogenic diols.

New nitrite ionic liquid (IL-ONO) and nanoparticles of organosilane-based nitrite ionic liquid immobilized on silica as nitrosonium sources for electrophilic aromatic nitrosation

Valizadeh, Hassan,Amiri, Mohammad,Shomali, Ashkan

experimental part, p. 1103 - 1108 (2012/03/10)

An improved method for the synthesis of nitrosoarenes has been developed using a new nitrite ionic liquid (IL-ONO) and immobilized nitrite ionic liquid. These ionic liquids play as nitrosonium sources for electrophilic aromatic nitrosation of active aromatics at 0-5 °C. Their action was accomplished in water and the satisfactory results were obtained under the mild conditions in short reaction time.

Nitrosation kinetics of phenolic components of foods and beverages

Paz Ferna?ndez-Liencres,Calle, Emilio,Gonza?lez-Mancebo, Samuel,Casado?, Julio,Quintero, Bartolome?

, p. 119 - 125 (2007/10/03)

The kinetics of the reactions between sodium nitrite and phenol or m-, o-, or p-cresol in potassium hydrogen phthalate buffers of pH 2.5-5.7 were determined by integration of the monitored absorbance of the C-nitroso reaction products. At pH > 3, the dominant reaction was C-nitrosation through a mechanism that appears to consist of a diffusion-controlled attack on the nitrosatable substrate by NO+/NO2H2+ ions followed by a slow proton transfer step; the latter step is supported by the observation of basic catalysis by the buffer which does not form alternative nitrosating agents as nitrosyl compounds. The catalytic coefficients of both anionic forms of the buffer have been determined. The observed order of substrate reactivities (o-cresol ≈ m-cresol > phenol ? p-cresol) is explained by the hyperconjugative effect of the methyl group in o- and m-cresol, and by its blocking the para position in p-cresol. Analysis of a plot of ΔH# against ΔS# shows that the reaction with p-cresol differs from those with o- and m-cresol as regards the formation and decomposition of the transition state. The genotoxicity of nitrosatable phenols is compared with their reactivity with NO+/NO2H2+.

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