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N-(4-AMINO-6,7-DIMETHOXYQUINAZOL-2-YL)-N-METHYL-2-CYANOETHYLAMINE is a chemical compound with the molecular structure characterized by a quinazoline core, featuring an amino group at the 4-position and methoxy groups at the 6 and 7 positions. It also has a cyanoethylamine side chain attached to the nitrogen atom. N-(4-AMINO-6,7-DIMETHOXYQUINAZOL-2-YL)-N-METHYL-2-CYANOETHYLAMINE is a white solid and is known for its potential applications in the pharmaceutical industry, particularly as an intermediate in the synthesis of Alfuzosin, a drug that acts as an α1-adrenoceptor antagonist.

76362-28-2

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76362-28-2 Usage

Uses

Used in Pharmaceutical Industry:
N-(4-AMINO-6,7-DIMETHOXYQUINAZOL-2-YL)-N-METHYL-2-CYANOETHYLAMINE is used as an intermediate in the synthesis of Alfuzosin, a medication that serves as a potential α1-adrenoceptor antagonist. Its role in the synthesis process is crucial for the development of this drug, which is used to treat various conditions related to prostate enlargement and other related urinary issues.
Used in Chemical Research:
As a chemical compound with unique structural features, N-(4-AMINO-6,7-DIMETHOXYQUINAZOL-2-YL)-N-METHYL-2-CYANOETHYLAMINE can also be utilized in chemical research for the exploration of new drug candidates, understanding its reactivity, and investigating its potential interactions with various biological targets. This can lead to the discovery of new therapeutic agents and a better understanding of its pharmacological properties.

Check Digit Verification of cas no

The CAS Registry Mumber 76362-28-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,3,6 and 2 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 76362-28:
(7*7)+(6*6)+(5*3)+(4*6)+(3*2)+(2*2)+(1*8)=142
142 % 10 = 2
So 76362-28-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H17N5O2/c1-19(6-4-5-15)14-17-10-8-12(21-3)11(20-2)7-9(10)13(16)18-14/h7-8H,4,6H2,1-3H3,(H2,16,17,18)

76362-28-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[(4-amino-6,7-dimethoxyquinazolin-2-yl)-methylamino]propanenitrile

1.2 Other means of identification

Product number -
Other names N-(4-amino-6,7-dimethoxy-quinazolin-2-yl)-N-methyl-2-cyanoethyl-amine

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:76362-28-2 SDS

76362-28-2Relevant academic research and scientific papers

PROCESS FOR PREPARING ALFUZOSIN

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Page/Page column 8, (2008/12/07)

Processes for preparing alfuzosin and pharmaceutically acceptable salts, solvates, hydrates thereof are disclosed. The present invention also discloses processes for preparation of anhydrous alfuzosin hydrochloride having substantially free from other pseudopolymorphic crystalline forms particularly dihydrate form of alfuzosin hydrochloride.

AN IMPROVED PROCESS FOR THE PREPARATION OF ALFUZOSIN HYDROCHLORIDE

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Page/Page column 7, (2009/03/07)

The present invention relates to an improved process for the preparation of Alfuzosin hydrochloride of formula (I) comprising a step of reacting compound of formula (IV) with compound of formula (V) in presence of aprotic solvent to obtain compound of formula (III) which is a useful intermediate for synthesis of Alfuzosin hydrochloride of formula (I).

PROCESS FOR THE PREPARATION OF ALFUZOSIN

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Page/Page column 7-8, (2008/06/13)

The present invention relates to an improved process for the preparation of N-[3-[(4-amino-6,7-dimethoxy-2-quinazolinyl)methylamino]propyl]tetrahydrofuran-2-carboxamide of Formula (I).

PROCESSES FOR THE PREPARATION OF ALFUZOSIN

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Page/Page column 8, (2008/06/13)

The invention relates to processes for the preparation of alfuzosin or pharmaceutically acceptable salts thereof in high purity. More particularly, it relates to the preparation of pure crystalline alfuzosin base. The invention also relates to pharmaceutical compositions that include the pure alfuzosin or a pharmaceutically acceptable salt thereof.

PROCESS FOR THE PREPARATION OF ALFUZOSIN

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Page/Page column 6, (2010/11/27)

The present invention relates to a simple process for the preparation of alfuzosin, it's bases and its pharmaceutically acceptable salts thereof.

PROCESSES FOR THE PREPARATION OF ALFUZOSIN AND SALTS THEREOF AND NOVEL CRYSTALLINE FORMS OF ALFUZOSIN

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Page/Page column 27, (2008/06/13)

The present invention provides novel crystalline forms of a.lfuzosin and alfuzosin hydrochloride and processes for their preparation. Also provided are pharmaceutical compositions containing the new crystalline forms.

4-Amino-6,7-dimethoxyquinazol-2-yl alkylenediamines

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, (2008/06/13)

Alkylenediamine amides corresponding to the general formula (I) STR1 in which R1 and R2 each represent, independently of one another, a hydrogen atom, an alkyl having 1 to 4 carbon atoms or the benzyl radical, n is equal to 2, 3 or 4 and R represents either a cycloalkyl radical having 3 to 6 carbon atoms, or a radical STR2 in which m is 0, 1 or 2, STR3 in which m is 0, 1 or 2 and p is 0, 1 or 2, and also their addition salts with pharmaceutically acceptable acids. These compounds may be prepared by reacting an aminoamide STR4 with a 4-amino-2-halogeno-6,7-dimethoxyquinazoline (II). The compounds are useful in treating cardiovascular disorders, and pharmaceutical compositions containing the compounds are also claimed.

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