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2-(Dimethylamino)-5-nitrobenzaldehyde is a yellow crystalline chemical compound with the chemical formula C9H10N2O3. It is known for its versatile applications in various industrial and research fields, including organic synthesis, pharmaceuticals, dyes, pesticides, and as a starting material for the production of other chemical compounds. Its potential biological and pharmacological activities also make it a compound of interest in medicine and biotechnology.

34601-40-6

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34601-40-6 Usage

Uses

Used in Organic Synthesis:
2-(Dimethylamino)-5-nitrobenzaldehyde is used as a reagent in organic synthesis for the preparation of various chemical compounds.
Used in Pharmaceutical Industry:
2-(Dimethylamino)-5-nitrobenzaldehyde is used as an intermediate in the production of pharmaceuticals, contributing to the development of new drugs.
Used in Dye Industry:
2-(Dimethylamino)-5-nitrobenzaldehyde is utilized in the manufacture of dyes, playing a crucial role in the coloration of various materials.
Used in Pesticide Industry:
2-(Dimethylamino)-5-nitrobenzaldehyde is employed in the production of certain pesticides, helping to create effective solutions for pest control.
Used in Chemical Research:
As a starting material, 2-(Dimethylamino)-5-nitrobenzaldehyde is used in the research and development of new chemical compounds, driving innovation in the chemical industry.
Used in Medicine and Biotechnology:
2-(Dimethylamino)-5-nitrobenzaldehyde is studied for its potential biological and pharmacological activities, indicating its potential use in the development of new therapeutic agents and biotechnological applications.

Check Digit Verification of cas no

The CAS Registry Mumber 34601-40-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,6,0 and 1 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 34601-40:
(7*3)+(6*4)+(5*6)+(4*0)+(3*1)+(2*4)+(1*0)=86
86 % 10 = 6
So 34601-40-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H10N2O3/c1-10(2)9-4-3-8(11(13)14)5-7(9)6-12/h3-6H,1-2H3

34601-40-6SDS

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 2-(dimethylamino)-5-nitrobenzaldehyde

1.2 Other means of identification

Product number -
Other names 2-dimethylamino-5-nitrobenzaldehyde

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:34601-40-6 SDS

34601-40-6Downstream Products

34601-40-6Relevant academic research and scientific papers

Directed Amination of Aryl Methyl Ethers Mediated by Ti(NMe2)4 at Room Temperature

Chen, Zhou,Liu, Jinna,Pei, Hao,Liu, Wei,Chen, Yanmei,Wu, Jian,Li, Wu,Li, Yahong

supporting information, p. 3406 - 3409 (2015/07/28)

An efficient C-O amination of aryl methyl ethers has been achieved. This transformation proceeds via imine-directed Ti(IV)-mediated cross-coupling reactions between aryl methyl ethers and Ti(NR2)4 at room temperature, straightforwardly leading to a series of arylamines. This protocol features a wide substrate scope, exclusive regioselectivity, and mild reaction conditions.

Interaction of barbituric acids with o-dialkylaminobenzaldehydes

Krasnov, Konstantin A.,Kartsev, Viktor G.,Khrustalev, Victor N.

, p. 52 - 54 (2007/10/03)

Barbituric or 2-thiobarbituric acids interact with o- dialkylaminobenzaldehydes to give 5-o-dialkylaminobenzylidene derivatives, which cyclise into 2,4,6-trioxoperhydropyrimidine-5-spiro-3′-(1′, 2′,3′,4′-tetrahydroquinolines) under mild conditions; the me

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