62936-64-5 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
These are alternative names for the compound, which describe its structure and functional groups.
Explanation
The physical appearance of the compound, indicating its color and state (solid, liquid, or gas).
Explanation
The primary applications of the compound in various industries, highlighting its importance in chemical processes.
Explanation
The mass of one mole of the compound, which is a measure of its size and can be used to calculate the mass of a given number of moles.
Explanation
The compound is classified as a nitrile due to the presence of a carbon-nitrogen triple bond (C≡N) in its structure.
Explanation
The compound should be handled with care and proper safety protocols should be followed to minimize the risk of exposure and potential health hazards.
Appearance
White to beige solid
Uses
Production of pharmaceuticals and organic synthesis
Molecular weight
225.03 grams per mole
Classification
Nitrile
Safety precautions
Potential toxicity and harmful effects if ingested, inhaled, or in contact with skin
Check Digit Verification of cas no
The CAS Registry Mumber 62936-64-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,9,3 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 62936-64:
(7*6)+(6*2)+(5*9)+(4*3)+(3*6)+(2*6)+(1*4)=145
145 % 10 = 5
So 62936-64-5 is a valid CAS Registry Number.
62936-64-5Relevant articles and documents
Utilization of ultrasonic irradiation as green and effective one-pot protocol to prepare a novel series of bis-2-amino-1, 3, 4-oxa(thia)diazoles and bis-tetrazoles
Arafa, Wael Abdelgayed Ahmed,Abdel-Magied, Ahmed Fawzy
, p. 327 - 340 (2017/12/06)
In an effective and straightforward conversion, bis-semicarbazones and bis-thiosemicarbazones are transformed into a diversity of novel substituted bis-2-amino-1, 3, 4-oxadiazoles and bis-2-amino-1, 3, 4-thiadiazoles, respectively under ultrasonic irradiation. Bis-tetrazoles are obtained from the dialdehydes by sequential reaction with hydroxylamine hydrochloride, phosphorus pentoxide and sodium azide without isolation of the intermediates oximes and nitriles. All the reactions proceed cleanly and smoothly under mild conditions, with short reaction times and broad functional groups possibility. No side reactions were observed.
