175731-00-7 Usage
Derivative of thiophene
A heterocyclic compound containing a sulfur atom 2-(dichloroMethyl)-3-nitrothiophene is derived from thiophene, which is a five-membered ring structure with one sulfur atom and four carbon atoms.
Nitro group
A functional group consisting of an oxygen and nitrogen atom (-NO2) The compound contains a nitro group, which is a common functional group in organic chemistry and can influence the reactivity and properties of the molecule.
Dichloromethyl group
A methyl group (CH3) with two chlorine atoms (Cl) attached The compound also contains a dichloroMethyl group, which is a halogenated alkyl group that can affect the molecule's reactivity and stability.
Use as an intermediate
Commonly used in the synthesis of various pharmaceuticals and agrochemicals 2-(dichloroMethyl)-3-nitrothiophene serves as a building block for the synthesis of other organic compounds, particularly in the pharmaceutical and agrochemical industries.
Potential applications
Organic chemistry building block for more complex molecules The compound has potential applications in the field of organic chemistry as a starting material for the synthesis of more complex molecules.
Safety precautions
Handle with care and follow safety protocols due to potential hazards Due to its potential hazards, it is important to handle 2-(dichloroMethyl)-3-nitrothiophene with care and follow appropriate safety protocols to minimize risks.
Check Digit Verification of cas no
The CAS Registry Mumber 175731-00-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,5,7,3 and 1 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 175731-00:
(8*1)+(7*7)+(6*5)+(5*7)+(4*3)+(3*1)+(2*0)+(1*0)=137
137 % 10 = 7
So 175731-00-7 is a valid CAS Registry Number.
175731-00-7Relevant articles and documents
A synthesis of fused pyrimidine mono-N-oxides
Ostrowski, Stanislaw
, p. 389 - 395 (2007/10/03)
An efficient synthesis of functionalized fused pyrimidine mono-N-oxide derivatives from the nitroaromatic compounds (involving the Vicarious Nucleophilic Substitution of Hydrogen and cyclocondensation of aromatic orthoaminooximes with orthoesters) is described.
