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Ethyl 5H-tetrazol-5-ylidenecarbamate is a chemical compound with the molecular formula C4H7N5O2. It is a derivative of the tetrazol-5-ylidenecarbamate class, characterized by the presence of a tetrazol ring and a carbamate group. ethyl 5H-tetrazol-5-ylidenecarbamate is known for its potential applications in various chemical and pharmaceutical processes, such as the synthesis of tetrazol-based compounds, which are often used in the development of drugs and other bioactive molecules. The ethyl group attached to the carbamate provides additional functionality and reactivity, making it a versatile building block in organic synthesis. Its properties, such as solubility and stability, can be tailored for specific applications, and it is often used in research and development to explore new chemical reactions and pathways.

5326-16-9

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5326-16-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5326-16-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,2 and 6 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5326-16:
(6*5)+(5*3)+(4*2)+(3*6)+(2*1)+(1*6)=79
79 % 10 = 9
So 5326-16-9 is a valid CAS Registry Number.

5326-16-9SDS

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 ethyl N-(2H-tetrazol-5-yl)carbamate

1.2 Other means of identification

Product number -
Other names (1H-tetrazol-5-yl)-carbamic acid ethyl ester

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:5326-16-9 SDS

5326-16-9Downstream Products

5326-16-9Relevant academic research and scientific papers

Method of producing alkyl substituted 5-amidotetrazoles

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, (2008/06/13)

In a process for the production of Alkyl substituted 5-amidotetrazole compounds represented by the formula: STR1 wherein A represents NHX or NRR' X represents a lower alkyl group R represents a lower alkyl group, and R' represents a lower alkyl group. reacts 5-aminotetrazole with an alkyl isocyanate or a dialkyl carbamoyl halide in a polar solvent.

Substituted 5-amidotetrazoles

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, (2008/06/13)

In a process for the production of cellular products comprising thermoplastic or rubber materials the blowing agents employed have the formula: STR1 wherein A represents NHX, NRR' or OR X represents H or a lower alkyl group, R represents a lower alkyl group, and R' represents a lower alkyl group. The novel blowing agents provide high gas yields and have high decomposition temperatures while forming only inert nitrogen gas. They are particularly suitable for the production of cellular products from high temperature thermoplastic materials such as polycarbonates.

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