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Benzenamine, N-(methoxymethyl)-4-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 88919-94-2 Structure
  • Basic information

    1. Product Name: Benzenamine, N-(methoxymethyl)-4-methyl-
    2. Synonyms:
    3. CAS NO:88919-94-2
    4. Molecular Formula: C9H13NO
    5. Molecular Weight: 151.208
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 88919-94-2.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: Benzenamine, N-(methoxymethyl)-4-methyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzenamine, N-(methoxymethyl)-4-methyl-(88919-94-2)
    11. EPA Substance Registry System: Benzenamine, N-(methoxymethyl)-4-methyl-(88919-94-2)
  • 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: 88919-94-2(Hazardous Substances Data)

88919-94-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88919-94-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,9,1 and 9 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 88919-94:
(7*8)+(6*8)+(5*9)+(4*1)+(3*9)+(2*9)+(1*4)=202
202 % 10 = 2
So 88919-94-2 is a valid CAS Registry Number.

88919-94-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(methoxymethyl)-4-methylaniline

1.2 Other means of identification

Product number -
Other names N-(Methoxymethyl)-p-anisidine

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:88919-94-2 SDS

88919-94-2Relevant articles and documents

P4VPy–CuO nanoparticles as a novel and reusable catalyst: application at the protection of alcohols, phenols and amines

Shirini, Farhad,Fallah-Shojaei, Abdollah,Abedini, Masoumeh,Samavi, Laleh

, p. 1699 - 1712 (2016/07/27)

P4VPy–CuO nanoparticles were synthesized using ultrasound irradiations. Relevant properties of the synthesized nanoparticles were investigated by X-ray diffraction, scanning electron microscopy, transmission electron microscopy and Fourier transform infrared spectroscopy. After identification, the prepared reagent was used for the promotion of different types of protection reactions of alcohols, phenols and amines. Easy workup, short reaction times, excellent yields, relatively low cost and reusability of the catalyst are the striking features of the reported methods.

Preparation of N,O-Aminals as Synthetic Equivalents of H2C=NAr and (H2C=NHAr)+ ions: Neutral- and Acid-promoted Transformations

Barluenga, Jose,Bayon, Ana M.,Campos, Pedro,Asensio, Gregorio,Gonzalez-Nunez, Elena,Molina, Yolanda

, p. 1631 - 1636 (2007/10/02)

A general method for the synthesis of N, O-aminals derived from primary aromatic amines is described.The reactivity of these compounds under neutral and acidic conditions has been studied and the title compounds can be envisaged as general purpose H2C=NAr or (H2C=NAr)+ equivalents.N,O-Aminals have been converted into perhydrotriazines by moderate heating and into bis(4-aminoaryl)methane derivatives or N-benzylarylamines, respectively, when heated in acidid media with pH control.Reduction od N,O-acetals with sodium cyanoborohydride has revealed that the C-O bond is broken exclusively in acidic media.

Monoalkylation of Primary Aromatic Amines via N-(Alkoxymethyl)aryl Amines. Evidence for the Formation of Stable Monomeric Methyleneamines

Barluenga, Jose,Bayon, Ana M.,Asensio, Gregorio

, p. 1109 - 1110 (2007/10/02)

Monomeric methyleneamines (1), formed from N-(alkoxymethyl)arylamines (3), are stable at -60 deg C and may be trapped with organometallic reagents to provide the N-alkylarylamines (7).

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