146853-20-5 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of 1,3-Benzodioxole, 5-nitroso-.
Explanation
The physical appearance of the compound, which is a yellow-colored solid with a crystalline structure.
Explanation
Nitroso compounds are a class of organic compounds containing a nitroso group (-N=O) bonded to a carbon atom.
Explanation
Nitroso compounds, including 1,3-Benzodioxole, 5-nitroso-, have a wide range of applications in various industries due to their unique chemical properties.
Explanation
Research has been conducted to explore the possible therapeutic uses of 1,3-Benzodioxole, 5-nitrosoin the treatment of different health conditions.
Explanation
Nitroso compounds, including 1,3-Benzodioxole, 5-nitroso-, can pose health risks if not handled properly, making it essential to follow safety protocols when working with this compound.
Explanation
Due to the potential toxicity and hazards associated with nitroso compounds, it is crucial to handle 1,3-Benzodioxole, 5-nitrosowith care and follow appropriate safety measures.
Appearance
Yellow crystalline solid
Classification
Nitroso compound
Applications
Pharmaceutical, pesticides, rubber and plastics additives
Potential medicinal properties
Studied for treatment of various health conditions
Toxicity
Can be toxic and potentially hazardous
Handling precautions
Careful handling required
Check Digit Verification of cas no
The CAS Registry Mumber 146853-20-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,8,5 and 3 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 146853-20:
(8*1)+(7*4)+(6*6)+(5*8)+(4*5)+(3*3)+(2*2)+(1*0)=145
145 % 10 = 5
So 146853-20-5 is a valid CAS Registry Number.
146853-20-5Relevant articles and documents
Synthesis of Nitrosobenzene Derivatives via Nitrosodesilylation Reaction
Kohlmeyer, Corinna,Klüppel, Maike,Hilt, Gerhard
, p. 3915 - 3920 (2018/04/14)
The electrophilic ipso-substitution of trimethylsilyl-substituted benzene derivatives into nitrosobenzene derivatives is reported. The optimization of the reaction conditions was performed for moderately electron-deficient, electron-rich, and sterically hindered starting materials by varying reaction time, temperature, and equivalents of NOBF4. Also, a stable intermediate of the nitrosation reaction could be characterized by 19F NMR which can be assigned to a NO+ adduct with the nitrosobenzene derivative. This complex decomposes upon aqueous workup and liberates the desired nitrosobenzene derivative.
Biocidal compounds
-
, (2008/06/13)
The invention provides compounds of general formula STR1 wherein m is 0 or 1; each of R1 and R2, and R3 and R4 if present, independently represents a hydrogen or halogen atom or an optionally substituted alkyl, cycloalkyl or aryl group, or R1 and R2 together or R3 and R4 together represent an optionally substituted alkylene chain; X represents a cyano group, a group --COOH or a salt, ester or amido derivative thereof; Y represents an alkyl group or a halogen atom; and n represents 0, 1, 2 or 3; a process for their preparation; compositions containing such compounds and their use as fungicides.
