849351-92-4 Usage
Purity
97%
Appearance
White to off-white crystalline solid
Molecular Weight
190.65 g/mol
Solubility
Soluble in organic solvents like DMF, DMSO, and ethanol
Reactivity
Highly reactive and selectively reacts with specific functional groups
Applications
a. Organic synthesis
b. Pharmaceutical research
c. Building block in the synthesis of pharmaceutical drugs
d. Synthesis of agrochemicals and other fine chemicals
Suitability
Ideal for research and development applications due to high purity
Storage
Should be stored in a cool, dry place, away from heat, light, and moisture
Safety Precautions
a. Use protective gloves and eyewear when handling
b. Avoid inhalation and ingestion
c. Dispose of according to local regulations and safety guidelines
Stability
Stable under normal laboratory conditions
Hazardous Decompostion Products
May produce toxic fumes when heated or exposed to flame
Melting Point
79-83°C (176.2-181.4°F)
Boiling Point
Not available, but it is expected to have a high boiling point due to its molecular structure
Density
Not available, but it is expected to be higher than water due to its molecular weight and structure
Flash Point
Not available, but it is expected to have a high flash point due to its stability under normal conditions
Vapor Pressure
Not available, but it is expected to have low vapor pressure due to its molecular weight and structure
Regulatory Information
Follow local and international regulations for handling, storage, and disposal of chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 849351-92-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,9,3,5 and 1 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 849351-92:
(8*8)+(7*4)+(6*9)+(5*3)+(4*5)+(3*1)+(2*9)+(1*2)=204
204 % 10 = 4
So 849351-92-4 is a valid CAS Registry Number.
849351-92-4Relevant academic research and scientific papers
Shafiee,Akbarzadeh,Foroumadi,Hadizadeh
, p. 141 - 144 (1998)
A series of isomeric 4 and 5-alkylsulfonyl, alkylsulfinylimidazoles 9, 10 were prepared by two general methods. Chlorosulfonation of imidazole afforded 4(5)-chlorosulfonylimidazoles 2, 4, 5. The chlorosulfonyl derivatives were reduced, alkylated and oxidi
