Cas 1449110-68-2,N-cinnamyl-N-(4-hydroxy-4-(2-hydroxyphenyl)but-2-yn-1-yl)-4-methylbenzenesulfonamide

1449110-68-2

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Basic information

Product Name: N-cinnamyl-N-(4-hydroxy-4-(2-hydroxyphenyl)but-2-yn-1-yl)-4-methylbenzenesulfonamide
Synonyms: N-cinnamyl-N-(4-hydroxy-4-(2-hydroxyphenyl)but-2-yn-1-yl)-4-methylbenzenesulfonamide
CAS NO:1449110-68-2
Molecular Formula:
Molecular Weight: 447.555
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: N-cinnamyl-N-(4-hydroxy-4-(2-hydroxyphenyl)but-2-yn-1-yl)-4-methylbenzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: N-cinnamyl-N-(4-hydroxy-4-(2-hydroxyphenyl)but-2-yn-1-yl)-4-methylbenzenesulfonamide(1449110-68-2)
EPA Substance Registry System: N-cinnamyl-N-(4-hydroxy-4-(2-hydroxyphenyl)but-2-yn-1-yl)-4-methylbenzenesulfonamide(1449110-68-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1449110-68-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1449110-68-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,9,1,1 and 0 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1449110-68:
(9*1)+(8*4)+(7*4)+(6*9)+(5*1)+(4*1)+(3*0)+(2*6)+(1*8)=152
152 % 10 = 2
So 1449110-68-2 is a valid CAS Registry Number.

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1449110-68-2Relevant academic research and scientific papers

Dual Catalysis: Proton/Metal-Catalyzed Tandem Benzofuran Annulation/Carbene Transfer Reaction

Ma, Jun,Chen, Kai,Fu, Hongguang,Zhang, Li,Wu, Wanqing,Jiang, Huanfeng,Zhu, Shifa

, p. 1322 - 1325 (2016)

An efficient proton/metal-catalyzed tandem benzofuran annulation/carbene transfer reaction for the synthesis of various benzofuryl-substituted cyclopropanes and cycloheptatrienes has been developed. The reaction was proposed to proceed through two key int

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