1445582-60-4 Usage
General Description
The chemical "(S)-1-(3,5-bis(trifluoroMethyl)phenyl)-3-(1-phenylethyl)thiourea" is a thiourea derivative with a molecular formula of C17H14F6N2S. It consists of a thiourea group, which is a sulfur-containing functional group, attached to a phenylethyl group and a trifluoromethylphenyl group. Thioureas are known for their diverse biological activities and are used in medicinal chemistry for the synthesis of various pharmaceuticals. This specific compound may have potential applications in the fields of medicinal chemistry and drug development due to its unique structure and properties. The stereochemistry of this compound, denoted by the (S) prefix, indicates that it has a specific spatial arrangement of atoms, which can influence its biological activity and interactions with other molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 1445582-60-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,5,5,8 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1445582-60:
(9*1)+(8*4)+(7*4)+(6*5)+(5*5)+(4*8)+(3*2)+(2*6)+(1*0)=174
174 % 10 = 4
So 1445582-60-4 is a valid CAS Registry Number.
1445582-60-4Relevant articles and documents
Asymmetric Hydroazidation of Nitroalkenes Promoted by a Secondary Amine-Thiourea Catalyst
Bellavista, Tiziana,Meninno, Sara,Lattanzi, Alessandra,Della Sala, Giorgio
, p. 3365 - 3373 (2015)
Chiral β-nitro azides are obtained by asymmetric addition of azides to nitroalkenes, with an enantioselectivity of up to 82% ee. The reaction, promoted by an easily accessible secondary amine-thiourea catalyst, is performed with azidotrimethylsilane in th
