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3398-07-0

2-Aminobenzaldehyde oxime is an organic compound with the chemical formula C7H8N2O. It is derived from 2-aminobenzaldehyde, where an oxime group (-NHOH) replaces one of the hydrogen atoms on the nitrogen atom. 2-AMINOBENZALDEHYDE OXIME is a colorless to pale yellow crystalline solid and is soluble in common organic solvents such as ethanol and acetone. It is used as an intermediate in the synthesis of various pharmaceuticals, dyes, and other organic compounds. 2-Aminobenzaldehyde oxime is also known for its potential applications in the field of materials science, particularly in the development of sensors and other electronic devices due to its unique chemical properties.

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  • 3398-07-0 Structure

  • Basic information

    1. Product Name: 2-AMINOBENZALDEHYDE OXIME
    2. Synonyms: 2-AMINOBENZALDEHYDE OXIME
    3. CAS NO:3398-07-0
    4. Molecular Formula: C7H8N2O
    5. Molecular Weight: 136.15
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 3398-07-0.mol

  • Chemical Properties

    1. Melting Point: 134-135 °C
    2. Boiling Point: 276.2±23.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.18±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 10.98±0.10(Predicted)
    10. CAS DataBase Reference: 2-AMINOBENZALDEHYDE OXIME(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-AMINOBENZALDEHYDE OXIME(3398-07-0)
    12. EPA Substance Registry System: 2-AMINOBENZALDEHYDE OXIME(3398-07-0)

  • 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: 3398-07-0(Hazardous Substances Data)

3398-07-0 Usage

Physical state

white to light yellow solid

Uses

chelating agent, particularly in metal ion removal and recovery processes

Ability

bind to metal ions, forming stable complexes

Applications

industrial and environmental applications, organic synthesis, production of pharmaceuticals

Studied properties

potential antioxidant and antimicrobial properties

Check Digit Verification of cas no

The CAS Registry Mumber 3398-07-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,9 and 8 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3398-07:
(6*3)+(5*3)+(4*9)+(3*8)+(2*0)+(1*7)=100
100 % 10 = 0
So 3398-07-0 is a valid CAS Registry Number.

3398-07-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-aminobenzaldehyde oxime

1.2 Other means of identification

Product number -
Other names 2-AMINOBENZALDEHYDE OXIME

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:3398-07-0 SDS

3398-07-0Relevant articles and documents

Eco-friendly H2O2 oxidation of 1,2-dihydroquinazoline-3-oxides to quinazoline-3-oxides

Samandram, Rashinikumar,?etin Koruk?u, Meliha,Co?kun, Necdet

supporting information, p. 2349 - 2356 (2021/06/14)

2-Aminobenzaldehyde, 1-(2-aminophenyl)ethanone, and 2-aminophenyl phenyl methanone oximes 1 were reacted with aromatic aldehydes to give the corresponding 1,2-dihydroquinazoline-3-oxides 2. The latter were converted in high yields to a series of quinazoli

Determination the structure of new some imines by physical and chemical methods

Al-Dabbagh, Asmaa B.,Othman, Arwa M.

, p. 6181 - 6194 (2021/11/08)

This paper is concerned with the preparation of eight new imines by standard methods; These having syn oxime and Schiff base structures. They are derived from aromatic aldehydes with suitable primary amines, depending on their structures. This investigati

An organocatalytic enantioselective direct α-heteroarylation of aldehydes with isoquinoline: N -oxides

Bertuzzi, Giulio,Pecorari, Daniel,Bernardi, Luca,Fochi, Mariafrancesca

supporting information, p. 3977 - 3980 (2018/04/23)

A new protocol for the enantioselective direct α-heteroarylation of aldehydes with isoquinoline N-oxides, via chiral enamine catalysis, has been successfully developed. High enantiomeric excesses and moderate to good yields were achieved for a variety of α-heteroarylated aldehydes.

A practical, metal-free synthesis of 1H-Lndazoles

Counceller, Carla M.,Eichman, Chad C.,Wray, Brertda C.,Stambuli, James P.

supporting information; experimental part, p. 1021 - 1023 (2009/04/07)

The synthesis of 1H-indazoles is achieved from o-aminobenzoximes by the selective activation of the oxime in the presence of the amino group. The reaction occurs with a variety of substituted o-aminobenzoximes using a slight excess of methanesulfonyl chloride and triethylamine at 0-23 °C and is amenable to scale-up. The synthesis of 1 H-indazoles under these conditions is extremely mild compared with previous synthetic approaches and affords the desired compounds in good to excellent yields.

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