185330-16-9 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule. In this case, 1,4-Benzenediol, 2-azidohas 6 carbon (C) atoms, 4 hydrogen (H) atoms, 2 nitrogen (N) atoms, and 2 oxygen (O) atoms.
Explanation
This is an alternative name for the compound, which highlights the presence of two hydroxyl (OH) groups and one azido (N3) group attached to a benzene ring.
Explanation
The compound's structure consists of a benzene ring, which is a six-carbon ring with alternating single and double bonds. Two of the carbons in the ring have hydroxyl groups attached, and one carbon has an azido group attached.
Explanation
1,4-Benzenediol, 2-azidois used in various chemical processes, including the synthesis of new compounds and materials. It is also utilized in the preparation of pharmaceuticals and dyes due to its unique chemical properties.
Structure
Benzene ring with two hydroxyl groups (OH) and one azido group (N3)
Applications
Chemical reactions, organic synthesis, pharmaceuticals, dyes
Potential uses
Photo-induced transformations, novel drug development
Check Digit Verification of cas no
The CAS Registry Mumber 185330-16-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,5,3,3 and 0 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 185330-16:
(8*1)+(7*8)+(6*5)+(5*3)+(4*3)+(3*0)+(2*1)+(1*6)=129
129 % 10 = 9
So 185330-16-9 is a valid CAS Registry Number.
185330-16-9Relevant academic research and scientific papers
Horn, Chris-Marie,Aucamp, Janine,Smit, Frans J.,Seldon, Ronnett,Jordaan, Audrey,Warner, Digby F.,N’Da, David D.
, p. 1387 - 1399 (2020)
Infectious diseases such as tuberculosis and leishmaniasis are leading causes of human death. One of the major factors contributing to the poor control of these diseases is primarily the reduced effectiveness of the existing chemotherapies as result of th
Efficient Synthesis of Aminonaphthoquinones and Azidobenzohydroquinones: Mechanistic Considerations of the Reaction of Hydrazoic Acid with Quinones. An Overview
Couladouros, Elias A.,Plyta, Zoi F.,Haroutounian, Serkos A.,Papageorgiou, Vassilios P.
, p. 6 - 10 (2007/10/03)
Parameters useful to predict and control the reaction outcome of conjugate addition of hydrazoic acid to quinones have been studied, and the optimum conditions for the efficient synthesis of aminonaphthoquinones and azidobenzohydroquinones are reported. The application of this reaction for the efficient formal synthesis of dephostatin is also presented.
