19922-85-1 Usage
Derivative of benzene
The compound is based on a benzene ring structure, with modifications made to it by attaching various groups.
Contains two chlorine atoms
The compound has two Cl atoms attached to the benzene ring, which may influence its reactivity and properties.
Contains an ethyl group
An alkyl group with two carbon atoms (C2H5) is attached to the benzene ring, contributing to the compound's structure.
Contains a sulfanyl group
A functional group with a sulfur atom bonded to a carbon atom (R-S-) is part of the compound, affecting its chemical properties.
Commonly used in organic synthesis
The compound is frequently used as a reactant or building block in the preparation of more complex organic molecules.
Intermediate in the production of agricultural and pharmaceutical products
The compound serves as a stepping stone or precursor in the synthesis of various products used in agriculture and pharmaceuticals.
Classified as a hazardous substance
Due to its potential dangers, the compound is categorized as hazardous, requiring proper handling and storage procedures.
Can cause skin irritation
Contact with the compound may result in redness, itching, or swelling of the skin.
Can cause eye irritation
Exposure to the compound may lead to eye discomfort, redness, or even damage.
Can cause respiratory irritation
Inhalation of the compound may result in coughing, shortness of breath, or irritation of the respiratory system.
Check Digit Verification of cas no
The CAS Registry Mumber 19922-85-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,9,2 and 2 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 19922-85:
(7*1)+(6*9)+(5*9)+(4*2)+(3*2)+(2*8)+(1*5)=141
141 % 10 = 1
So 19922-85-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H10Cl2S/c10-5-6-12-7-8-3-1-2-4-9(8)11/h1-4H,5-7H2
19922-85-1Relevant articles and documents
As-triazine derivatives with potential therapeutic action. XXIX: Synthesis of 5-[2-(halogenobenzylthio)-ethyl]thio-6-azauracil derivatives as potential antiviral agents
Czobor, Francisc,Cristescu, Carol
, p. 1007 - 1011 (2007/10/03)
Several 2-chloroethyl-halogenobenzyl sulfides were obtained by the alkylation of sodated 2-mercaptoethanol with the corresponding halogenobenzyl halides. They reacted in hydroalcoholic medium with the sodium salt of 5-mercapto-6-azauracil to give the title compounds in 55-73% yield.
