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4-Guanidinobenzoyl Chloride, Hydrochloride (CAS# 7035-79-2) is an organic compound that serves as a versatile reagent in various chemical reactions and organic synthesis processes. It is characterized by its guanidino and benzoyl chloride functional groups, which contribute to its reactivity and potential applications in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.

7035-79-2

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7035-79-2 Usage

Uses

Used in Pharmaceutical Industry:
4-Guanidinobenzoyl Chloride, Hydrochloride is used as a synthetic intermediate for the development of various pharmaceutical compounds. Its reactivity allows for the formation of amide and urea linkages, which are common structural elements in many drug molecules. This makes it a valuable building block in the synthesis of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 4-Guanidinobenzoyl Chloride, Hydrochloride is utilized as a key component in the synthesis of active ingredients for pesticides and herbicides. Its ability to form stable chemical bonds with other molecules enables the creation of effective and targeted agrochemicals that can protect crops and enhance agricultural productivity.
Used in Organic Synthesis:
4-Guanidinobenzoyl Chloride, Hydrochloride is employed as a reagent in organic synthesis for the preparation of a wide range of specialty chemicals. Its unique functional groups facilitate various chemical reactions, such as acylation, amidation, and urea formation, which are essential for the synthesis of complex organic molecules with diverse applications in industries like materials science, coatings, and polymers.
Used in Research and Development:
4-Guanidinobenzoyl Chloride, Hydrochloride is also used in research and development settings to explore new chemical reactions and synthetic pathways. Its versatility as a reagent allows chemists to investigate novel approaches to the synthesis of biologically active compounds, new materials, and other specialty chemicals that can address various challenges in science and technology.

Check Digit Verification of cas no

The CAS Registry Mumber 7035-79-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,3 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7035-79:
(6*7)+(5*0)+(4*3)+(3*5)+(2*7)+(1*9)=92
92 % 10 = 2
So 7035-79-2 is a valid CAS Registry Number.

7035-79-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(diaminomethylideneamino)benzoyl chloride,hydrochloride

1.2 Other means of identification

Product number -
Other names 4-Guanidinobenzoyl Chloride,Hydrochloride

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:7035-79-2 SDS

7035-79-2Relevant academic research and scientific papers

Antineoplastic drugs with bipolar toxification/detoxification functionalities

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, (2008/06/13)

The composition, methods of synthesis, and applications of a new class of tumor selective antineoplastic drugs is described. These novel antineoplastic agents are of the general structure: A-C-B. The agents are designed with two key functionalities: a tri

AMIDINE COMPOUND

-

, (2008/06/13)

Amidino compounds represented by the formula STR1 and pharmaceutically acceptable acid addition salts thereof are novel compounds and are useful as powerful antitrypsine, antiplasmin, antikallikrein and antithrombin agents. Having strong anti-C1 (C1r, C1s) activities and an anticomplement activity, they are also useful as anticomplement agents. These amidino compounds are prepared by usual esterification of carboxylic acid compounds represented by the formula STR2 with 6-amidino-2-naphthol and, if necessary, can be transformed into pharmaceuticlly acceptable acid addition salts thereof.

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