25457-95-8 Usage
Molecular structure
2-methylpropan-1-ol backbone The basic structure of the compound is derived from propanol, with a 2-methylpropan-1-ol backbone serving as the foundation.
Amino group attachment
[(E)-(4-chlorophenyl)methylidene]amino An amino group is attached to the 2-methylpropan-1-ol backbone through a methylidene group and a 4-chlorophenyl group.
Chlorine atom presence
4-chlorophenyl group The compound contains a chlorophenyl group, which may impact its reactivity and biological properties.
Methylidene group
(E)-(4-chlorophenyl)methylidene A methylidene group is present in the compound, connecting the amino group to the 4-chlorophenyl group.
Stereochemistry
(E) configuration The compound has an (E) configuration, indicating the relative positions of the substituents around the double bond in the methylidene group.
Potential applications
Pharmaceutical or material science Due to its unique structure and functional groups, the compound may be of interest for further research and potential applications in various fields, such as pharmaceuticals or material science.
Molecular weight
233.74 g/mol The molecular weight of the compound is approximately 233.74 grams per mole.
Polarity
Polar The presence of the amino and methylidene groups suggests that the compound is polar, which may influence its solubility and interactions with other molecules and biological systems.
Check Digit Verification of cas no
The CAS Registry Mumber 25457-95-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,4,5 and 7 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 25457-95:
(7*2)+(6*5)+(5*4)+(4*5)+(3*7)+(2*9)+(1*5)=128
128 % 10 = 8
So 25457-95-8 is a valid CAS Registry Number.
25457-95-8Relevant articles and documents
Use of Hypervalent Iodine in the Synthesis of Isomeric Dihydrooxazoles
Carlucci, Claudia,Tota, Arianna,Colella, Marco,Ronamazzi, Giuseppe,Clarkson, Guy J.,Luisi, Renzo,Degennaro, Leonardo
, p. 428 - 436 (2018/06/11)
[Figure not available: see fulltext.] A convenient synthesis of 2- and/or 3-oxazolines has been developed depending on the structure and stereochemistry of the starting amino alcohol. PhI(OAc)2 acted as oxidant on the intermediate imine, as sup
HYDROXY SCHIFF BASE-OXAZOLIDINE TAUTOMERISM: APPARENT BREAKDOWN OF BALDWIN'S RULES
Astudillo, Mario E. Alva,Chokotho, Norris C. J.,Jarvis, Terence C.,Johnson, C. David,Lewis, Colin C.,McDonnell, Peter D.
, p. 5919 - 5928 (2007/10/02)
The tautomerism between hydroxy Schiff bases, X=C6H4CR=NCMe2CH2OH (R=H, Me, C6H5; X is a range of substituents) and X=C6H4CR=NC6H4(o-CH2OH), and the corresponding ring closed systems, oxazolidines and dihydrobenzoxazines, has been investigated.In all case
