64381-88-0 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
Synonyms are alternative names for a chemical compound, which can be used interchangeably.
Explanation
The compound is used as a starting material or building block in the synthesis of other chemicals, specifically dyes and pharmaceuticals.
Explanation
The compound exists in a solid state and has a yellow color.
Explanation
The compound can cause irritation to the skin and eyes upon contact. It also has the potential to cause cancer, making it a hazardous substance.
Explanation
Due to its toxic and harmful properties, the compound should be handled with care, using appropriate safety measures. It should only be used in controlled industrial or laboratory settings and under the supervision of trained professionals to minimize risks.
Explanation
The compound is classified as toxic and harmful due to its potential to cause harm to human health and the environment.
Synonyms
3-Methoxy-5-nitrobenzene-1,2-diamine
Usage
Intermediate in the production of dyes and pharmaceuticals
Physical state
Yellow solid
Hazardous properties
Skin and eye irritant, potential carcinogen
Precautions
Proper handling, controlled settings, trained professionals
Classification
Toxic and harmful chemical
Check Digit Verification of cas no
The CAS Registry Mumber 64381-88-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,3,8 and 1 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 64381-88:
(7*6)+(6*4)+(5*3)+(4*8)+(3*1)+(2*8)+(1*8)=140
140 % 10 = 0
So 64381-88-0 is a valid CAS Registry Number.
64381-88-0Relevant academic research and scientific papers
An efficient one-pot synthesis of aminobenzimidazoles
Fouchard, David M. D.,Tillekeratne, L. M. Viranga,Hudson, Richard A.
, p. 17 - 18 (2007/10/03)
An efficient one-pot procedure for the preparation of aminobenzimidazoles from dinitroaniline derivatives is described. The process helps to avoid the troublesome acetonitrile-mediated reductive ethylation reaction.
