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(4-Methoxy-benzyl)-(3-phenylsulfanyl-prop-2-ynyl)-amine is a complex organic compound with the molecular formula C21H19NO2S. It features a 4-methoxy-benzyl group, which is a benzyl group with a methoxy substituent at the para position, and a 3-phenylsulfanyl-prop-2-ynyl group, which is a propargyl group with a phenylsulfanyl substituent at the 3-position. (4-Methoxy-benzyl)-(3-phenylsulfanyl-prop-2-ynyl)-amine is characterized by its unique structure, which combines an aromatic benzene ring, an alkyne group, and a sulfanyl group, making it a potential candidate for various chemical reactions and applications in the fields of pharmaceuticals, materials science, and organic synthesis.

98729-73-8

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98729-73-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 98729-73-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,7,2 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 98729-73:
(7*9)+(6*8)+(5*7)+(4*2)+(3*9)+(2*7)+(1*3)=198
198 % 10 = 8
So 98729-73-8 is a valid CAS Registry Number.

98729-73-8Relevant academic research and scientific papers

CYCLIZATION REACTION OF N-PROPARGYL EPOXYAMIDE TO ACETYLENIC 2-AZETIDINONE, A PRECURSOR TO THIENAMYCIN AND RELATED CARBAPENEMS

Marayuma, Hiroshi,Shiozaki, Masao,Oida, Sadao,Hiraoka, Tetsuo

, p. 4521 - 4522 (2007/10/02)

Base treatment of N-propargyl epoxyamide 5 afforded the acetylenic 3-(hydroxyethyl)-2-azetidinone 9a, which was subsequently transformed to phenyl thiolester 2, a versatile intermediate for the carbapenem synthesis.

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