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Benzaldehyde, 4-amino-3,5-dimethyl(9CI) is a chemical compound characterized by the molecular formula C9H11NO. It features a benzene ring with an aldehyde and an amino group, along with two methyl groups. Known for its almond-like odor, Benzaldehyde, 4-amino-3,5-dimethyl- (9CI) is a versatile precursor in the synthesis of pharmaceuticals, dyes, and flavors, and is extensively utilized in the fragrance industry.

56066-83-2

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56066-83-2 Usage

Uses

Used in Pharmaceutical Industry:
Benzaldehyde, 4-amino-3,5-dimethyl(9CI) is used as a precursor in the synthesis of various pharmaceuticals for its ability to contribute to the development of new medicinal compounds.
Used in Dye Industry:
In the dye industry, Benzaldehyde, 4-amino-3,5-dimethyl(9CI) is utilized as a starting material for the production of dyes, leveraging its chemical structure to create a range of colorants.
Used in Flavor Industry:
Benzaldehyde, 4-amino-3,5-dimethyl(9CI) is employed as a flavoring agent, capitalizing on its almond-like aroma to enhance the taste profiles of various food products.
Used in Fragrance Industry:
Benzaldehyde, 4-amino-3,5-dimethyl(9CI) is used as a key ingredient in the fragrance industry, where its distinctive scent is incorporated into perfumes and other scented products to create desirable olfactory effects.
Used in Organic Chemistry as a Reagent:
Benzaldehyde, 4-amino-3,5-dimethyl(9CI) is used as a reagent in organic chemistry reactions, particularly in the synthesis of heterocycles and other complex organic compounds, due to its reactive functional groups.
Used in Research for Biological and Pharmacological Activities:
It is also studied for potential biological and pharmacological activities, indicating its use in scientific research to explore its effects on living organisms and its possible applications in medicine.

Check Digit Verification of cas no

The CAS Registry Mumber 56066-83-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,0,6 and 6 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 56066-83:
(7*5)+(6*6)+(5*0)+(4*6)+(3*6)+(2*8)+(1*3)=132
132 % 10 = 2
So 56066-83-2 is a valid CAS Registry Number.

56066-83-2SDS

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 4-Amino-3,5-dimethylbenzaldehyde

1.2 Other means of identification

Product number -
Other names 4-Amino-3.5-dimethyl-benzaldehyd

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:56066-83-2 SDS

56066-83-2Relevant academic research and scientific papers

Monitoring Ligand Substitution in (Catalytically Active) Metal Complexes with Bodipy-Tagged Diimines and NHC Ligands

Halter, Oliver,Spielmann, Jonas,Kanai, Yuki,Plenio, Herbert

, p. 2138 - 2149 (2019)

The reaction of 2,6-dimethyl-4-(Bodipy-8-yl)aniline with 1,4-dioxane-2,3-diol provides the respective diimine 3, followed by ring closure with paraformaldehyde, resulting in the imidazolium salt 4·HCl containing two fluorophores. The NHC metal complexes (

Synthetic method of rilpivirine intermediate

-

Paragraph 0026-0028; 0031-0032, (2020/07/12)

The invention provides a synthetic method of a rilpivirine intermediate. The synthesis method includes: taking 2, 4, 6-trimethylaniline as the raw material to react with 2, 3-dichloro-5, 6-dicyanobenzoquinone (DDQ) in a diluted hydrochloric acid solution

Pyrimidine heterocyclic compounds, pyrimidine heterocyclic compound salts, and preparation method and application thereof

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Paragraph 0243; 0244; 0245; 0246, (2017/07/26)

The invention provides pyrimidine heterocyclic compounds, pyrimidine heterocyclic compound salts, and a preparation method and application thereof. According to the pyrimidine heterocyclic compounds provided by the invention, specific Rq is selected, so that the obtained compounds have favorable drug resistance and long half life when being used as the medicine for treating or preventing HIV. The compounds have the advantages of high activity, low toxicity and high stability.

Regiospecific oxidation of an alkyl group of aromatic amine to carbonyl group by DDQ in aq. medium

Mane, Madhav S.,Balaskar, Ravi S.,Gavade, Sandip N.,Pabrekar, Pramod N.,Shingare, Murlidhar S.,Mane, Dhananjay V.

experimental part, p. 1039 - 1042 (2012/06/01)

The regiospecific oxidation of alkyl group of both sterically hindered and unhindered aromatic amine to corresponding carbonyl compound was done in aq. medium by using DDQ. The optimized reaction protocol was found to be most simple, high yielding and novel method for oxidation of alkyl group of aromatic amine in to its carbonyl compound.

Hydrogenated Benzo (C) Thiophene Derivatives as Immunomodulators

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Page/Page column 18, (2008/12/07)

The invention relates to novel thiophene derivatives, their preparation and their use as pharmaceutically active compounds. Said compounds particularly act as immunosuppressive agents.

COMPOUNDS FOR THE PREVENTION AND TREATMENT OF CARDIOVASCULAR DISEASES

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Page/Page column 45, (2008/12/07)

The present disclosure relates to compounds, which are useful for regulating the expression of apolipoprotein A-I (ApoA-I), and their use for treatment and prevention of cardiovascular disease and related disease states, including cholesterol- or lipid-related disorders, such as, for example, atherosclerosis.

HYDROGENATED BENZO (C) THIOPHENE DERIVATIVES AS IMMUNOMODULATORS

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Page/Page column 50, (2010/11/24)

The invention relates to novel thiophene derivatives, their preparation and their use as pharmaceutically active compounds. Said compounds particularly act as immunosuppressive agents.

Simple Synthetic Route to 4-Aminobenzaldehydes from Anilines

Liedholm, Brita

, p. 2235 - 2242 (2007/10/02)

Anilines unsubstituted at the 4-position react under mild conditions in Me2SO-HCl solvent (H+ = 0.6 mol dm-3) to give substituted 4-aminobenzaldehydes in high yields; although addition of CuCl2 gives a cleaner product, it is not esse

2,4-Diamino-5-(4-amino and 4-dimethylamino-3,5-dimethoxy benzyl)pyrimidines

-

, (2008/06/13)

2,4-Diamino-5-benzylpyrimidines of the formula STR1 wherein R1, R2, A, Z and n are as hereinafter set forth, are described. The 2,4-diamino-5-benzylpyrimidines of the invention have useful antibacterial activity. More particularly, t

REGIOSPECIFIC OXIDATION BY DDQ OF UNHINDERED ALKYL GROUPS IN STERICALLY HINDERED AROMATIC AMINES

Lal, Bansi,Gidwani, Ramesh M.,Reden, Jurgen,Souza, Noel J. de

, p. 2901 - 2904 (2007/10/02)

DDQ oxidises an unhindered activated alkyl group to a carbonyl or a hydroxymethyl group depending on the nature of the substitution, in a sterically hindered aromatic amine.

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