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Naphthalene-1-carbaldehyde 4-benzyl-thiosemicarbazone is a complex organic compound with the chemical formula C20H17N3S. It is derived from naphthalene, a polycyclic aromatic hydrocarbon, and features a thiosemicarbazone functional group, which is a sulfur-containing analog of the semicarbazone group. naphthalene-1-carbaldehyde 4-benzyl-thiosemicarbazone is known for its potential applications in coordination chemistry, particularly as a ligand in the formation of metal complexes. It is also of interest in the field of analytical chemistry for its use as a reagent in the detection and quantification of metal ions. The compound's structure and properties make it a valuable tool in research and development, although its use is primarily confined to laboratory settings due to its complex nature and potential toxicity.

7701-14-6

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7701-14-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7701-14-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,0 and 1 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7701-14:
(6*7)+(5*7)+(4*0)+(3*1)+(2*1)+(1*4)=86
86 % 10 = 6
So 7701-14-6 is a valid CAS Registry Number.

7701-14-6Relevant academic research and scientific papers

Structure-activity relationship of naphthaldehydethiosemicarbazones in melanogenesis inhibition

Thanigaimalai, Pillaiyar,Rao, Eeda Venkateswara,Lee, Ki-Cheul,Sharma, Vinay K.,Roh, Eunmiri,Kim, Youngsoo,Jung, Sang-Hun

scheme or table, p. 886 - 889 (2012/03/26)

2-(Naphthalen-1-ylmethylene)hydrazinecarbothioamide (14, IC50 = 1.1 μM) was discovered as a highly potent inhibitor of melanogenesis. To define the role of hydrogens (at N1 and N3) and sulfur in 14, a series of analogs 15a-p were synthesized an

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