64485-31-0 Usage
Nitroaromatic compound
A class of compounds that contain a nitro group (-NO2) attached to a benzene ring.
Nitro group
A functional group consisting of an oxygen atom and a nitrogen atom (-NO2), which is known for its high reactivity and explosive properties.
Benzene ring
A six-carbon ring structure with alternating single and double bonds, which is a fundamental structure in organic chemistry and aromatic compounds.
2-(Phenylsulfanyl)ethoxy group
A functional group composed of a sulfur atom bonded to a phenyl group (a six-carbon ring with alternating single and double bonds) and an ethoxy group (an ethyl group attached to an oxygen atom).
Intermediate in synthesis
A chemical species that is used in the preparation of other compounds and is typically not isolated or purified.
Reactivity
The compound's tendency to undergo chemical reactions and form new bonds, which is useful in organic synthesis reactions.
Introducing 2-(phenylsulfanyl)ethoxy group
The ability of the compound to transfer the 2-(phenylsulfanyl)ethoxy group to other organic molecules during chemical reactions.
Potential toxicity
The possibility that the compound may cause harm to living organisms upon exposure.
Environmental hazards
The potential for the compound to cause damage to the environment, such as contamination of water or soil.
Check Digit Verification of cas no
The CAS Registry Mumber 64485-31-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,4,8 and 5 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 64485-31:
(7*6)+(6*4)+(5*4)+(4*8)+(3*5)+(2*3)+(1*1)=140
140 % 10 = 0
So 64485-31-0 is a valid CAS Registry Number.
64485-31-0Relevant articles and documents
Solvent and crown ether/cryptand effects on the oximate-promoted 1,2-elimination from β-phenylmercaptoethyl p-nitrophenolate. Formation and reactivity of a crown ether-complexed potassium oximate ion pair
Buncel, Erwin,Kumar, Anurag,Xie, Hai-Qi,Moir, Robert Y.,Purdon, J. Garfield
, p. 437 - 447 (2007/10/02)
The reactions of β-phenylmercaptoethyl p-nitrophenolate (1) with three potassium oximates, viz. potassium 2,3-butanedione monoximate (BDOK), acetophenone oximate (APOK), and acetone oximate (AOK) have been investigated in two nonhydroxylic dipolar aprotic
