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63302-43-2

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63302-43-2 Usage

Description

1,4-Benzenediamine, N-(1,4-dimethylpentyl)is an organic compound with the molecular formula C11H20N2. It is a derivative of 1,4-benzenediamine, featuring a 1,4-dimethylpentyl group attached to the nitrogen atom. This modification enhances its reactivity and solubility in various solvents, making it a versatile building block for the synthesis of complex organic molecules.

Uses

1. Used in Chemical Synthesis:
1,4-Benzenediamine, N-(1,4-dimethylpentyl)is used as a reactant in the one-pot reductive alkylation of diamines. This process involves the condensation of two molecules of a primary amine with an aldehyde or ketone in the presence of a reducing agent, leading to the formation of a symmetrical diarylamine. The presence of the 1,4-dimethylpentyl group in this compound enhances its reactivity and selectivity in the reductive alkylation process, making it a valuable intermediate for the synthesis of various organic compounds.
2. Used in Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, 1,4-Benzenediamine, N-(1,4-dimethylpentyl)can potentially be used in the pharmaceutical industry as a building block for the development of novel drugs. Its unique structure and reactivity may allow for the creation of new drug candidates with improved pharmacological properties, such as increased potency, selectivity, and bioavailability.
3. Used in Material Science:
The unique structure of 1,4-Benzenediamine, N-(1,4-dimethylpentyl)may also find applications in the field of material science. Its ability to form covalent bonds with other molecules can be exploited to create new materials with specific properties, such as enhanced mechanical strength, thermal stability, or electrical conductivity. These materials could be used in various applications, including aerospace, automotive, and electronics industries.

Check Digit Verification of cas no

The CAS Registry Mumber 63302-43-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,3,0 and 2 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 63302-43:
(7*6)+(6*3)+(5*3)+(4*0)+(3*2)+(2*4)+(1*3)=92
92 % 10 = 2
So 63302-43-2 is a valid CAS Registry Number.
InChI:InChI=1/C13H22N2/c1-10(2)4-5-11(3)15-13-8-6-12(14)7-9-13/h6-11,15H,4-5,14H2,1-3H3

63302-43-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-N-(5-methylhexan-2-yl)benzene-1,4-diamine

1.2 Other means of identification

Product number -
Other names N-(1,4-dimethylpentyl)-p-phenylenediamine

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:63302-43-2 SDS

63302-43-2Relevant articles and documents

Preparation method of 2, 4, 6-tri(N-1, 4-dimethylamyl-p-phenylenediamine)-1, 3, 5-triazine

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Paragraph 0023-0024; 0026-0027; 0029-0030; 0032-0033; ...., (2021/11/26)

The invention discloses a preparation method of 2, 4, 6-tri(N-1, 4-dimethylamyl-p-phenylenediamine)-1, 3, 5-triazine. The preparation method comprises the following steps: carrying out catalytic hydrogenation reaction on p-aminoacetanilide and methyl isoamyl ketone to obtain N-1, 4-dimethylamyl-p-acetanilide; removing acetyl from N-1, 4-dimethylamyl-p-acetanilide in an alkali solution, so as to obtain N-1, 4-dimethylamyl-p-aniline; and carrying out substitution reaction on cyanuric chloride and N-1, 4-dimethylamyl-p-phenylenediamine, and carrying out after-treatment to obtain the 2, 4, 6-tri(N-1, 4-dimethylamyl-p-phenylenediamine)-1, 3, 5-triazine. The method has the advantages of high reaction selectivity and yield, few byproducts, low cost and good quality.

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