3375-37-9 Usage
Uses
Used in Organic Synthesis:
(2E)-1-(2,4-dinitrophenyl)-2-(1-phenylpropylidene)hydrazine is used as a versatile intermediate in organic synthesis for the development of various chemical compounds. Its hydrazine and dinitrophenyl groups facilitate a range of chemical transformations, making it a valuable component in the synthesis of complex organic molecules.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (2E)-1-(2,4-dinitrophenyl)-2-(1-phenylpropylidene)hydrazine is utilized as a building block for the design and synthesis of bioactive molecules. Its structural features and functional groups contribute to the development of molecules with potential therapeutic applications, offering a promising avenue for the creation of new pharmaceutical agents.
Used in Pharmaceutical Development:
(2E)-1-(2,4-dinitrophenyl)-2-(1-phenylpropylidene)hydrazine is employed as a key component in the development of pharmaceuticals, particularly for molecules with potential pharmacological activities. Its unique structure and functional groups enable the creation of novel drug candidates that can be further optimized for specific therapeutic targets and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 3375-37-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,7 and 5 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3375-37:
(6*3)+(5*3)+(4*7)+(3*5)+(2*3)+(1*7)=89
89 % 10 = 9
So 3375-37-9 is a valid CAS Registry Number.
3375-37-9Relevant academic research and scientific papers
The Synthesis of Ketones via α-Silyl Sulphides
Ager, David J.
, p. 195 - 204 (2007/10/02)
α-Phenylthiosilanes (2) have been prepared by alkylation of the anion (4) derived from the 1-phenylthio-1-trimethylsilylalkane (1).These anions (4) have benn prepared by a variety of methods including, direct deprotonation of (1), displacement of a phenylthio group by lithium naphthalenide addition of an alkyl-lithium to 1-phenylthio-1-trimethylsilylethene (7), and transmetallation of a tributylstannyl moiety.The formation of an alkyl-lithium by reaction of lithium naphthalenide with a phenyl sulphide provided an additional route to (2) from bis(phenylthio)acetals (8).An alternative path to the α-phenylthiosilanes (2) was to reduce the corresponding α-phenylsulphonylsilane (15); these, in turn, being readily available from alkylation or silylation of α-sulphonyl anions.The α-phenylthiosilanes (2) were converted into the O-trimethylsilylphenylthioacetal (18) by the sila-Pummerer rearrangement, although this was complicated by vinyl sulphide (20) formation in certain cases.Subsequent hydrolysis of (18) and (20) gave the ketone (3).
