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Hydroxyethylanisol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 125418-72-6 Structure
  • Basic information

    1. Product Name: Hydroxyethylanisol
    2. Synonyms: Hydroxyethylanisol;2-(4-Methoxy-3-nitroanilino)ethan-1-ol, N-(2-Hydroxyethyl)-4-methoxy-3-nitroaniline;2-[(4-Methoxy-3-nitrophenyl)amino]ethan-1-ol
    3. CAS NO:125418-72-6
    4. Molecular Formula: C9H12N2O4
    5. Molecular Weight: 212.2
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 125418-72-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 420.2°C at 760 mmHg
    3. Flash Point: 207.9°C
    4. Appearance: /
    5. Density: 1.336g/cm3
    6. Vapor Pressure: 8.19E-08mmHg at 25°C
    7. Refractive Index: 1.612
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: Hydroxyethylanisol(CAS DataBase Reference)
    11. NIST Chemistry Reference: Hydroxyethylanisol(125418-72-6)
    12. EPA Substance Registry System: Hydroxyethylanisol(125418-72-6)
  • 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: 125418-72-6(Hazardous Substances Data)

125418-72-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 125418-72-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,4,1 and 8 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 125418-72:
(8*1)+(7*2)+(6*5)+(5*4)+(4*1)+(3*8)+(2*7)+(1*2)=116
116 % 10 = 6
So 125418-72-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H12N2O4/c1-15-9-3-2-7(10-4-5-12)6-8(9)11(13)14/h2-3,6,10,12H,4-5H2,1H3

125418-72-6Downstream Products

125418-72-6Relevant articles and documents

2-amino-4 - (β-hydroxyethyl amino) anisole and its sulphate preparation method

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, (2017/04/06)

The invention relates to 2-amino-4-(beta-hydroxyethylamino) methoxybenzene and a preparation method of 2-amino-4-(beta-hydroxyethylamino) methoxybenzene sulfate. The preparation method comprises the steps as follows: 3-nitro-para-fluoroaniline is adopted as a raw material and subjected to nucleophilic substitution to produce 3-nitro-4-anisidine; 3-nitro-4-anisidine and chloroethyl chloroformate are subjected to condensation to synthesize 2-nitro-4-(beta-hydroxyethylamino) methoxybenzene with a hydrolysis and decarboxylation one-pot method; and 2-nitro-4-(beta-hydroxyethylamino) methoxybenzene has the hydrogenation reduction reaction to obtain a target product 2-amino-4-(beta-hydroxyethylamino) methoxybenzene which reacts with sulfate salt to obtain 2-amino-4-(beta-hydroxyethylamino) methoxybenzene sulfate. 2-amino-4-(beta-hydroxyethylamino) methoxybenzene and the preparation method of 2-amino-4-(beta-hydroxyethylamino) methoxybenzene sulfate have the advantages of high product quality, good yield, stable technology, small emission of three wastes, low cost, good economic efficiency and the like, and synthesis materials are easy to obtain.

New process for the preparation of 4-hydroxalkylamino-2-nitro-anisoles

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Page/Page column 2-3, (2008/06/13)

A process for the preparation of 4-hydroxyalkylamino-2-nitro-anisoles of the general formula (I) wherein m is 2 or 3; by reaction of a 4-halogeno-3-nitro-aniline of formula (II) with a chloroalkyl-chloroformate of formula (III), alkaline ring closure of t

Process for the preparation of hydroxyalkylaminonitrobenzene derivatives

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, (2008/06/13)

The present invention relates to a process for the preparation of compounds of the general formula I STR1 by reaction of compounds of the general formula II STR2 with compounds of the general formula III STR3 in inert aprotic solvents in the presence of a base and subsequent rearrangement of the resulting intermediate compound with an alkali metal hydroxide, characterized in that the intermediate compound is not isolated.

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