Cas 1361996-67-9,4-methyl-N-(1,1,1-trifluoro-3-iodo-4-oxo-4-phenylbutan-2-yl)benzenesulfonamide

1361996-67-9

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Basic information

Product Name: 4-methyl-N-(1,1,1-trifluoro-3-iodo-4-oxo-4-phenylbutan-2-yl)benzenesulfonamide
Synonyms: 4-methyl-N-(1,1,1-trifluoro-3-iodo-4-oxo-4-phenylbutan-2-yl)benzenesulfonamide
CAS NO:1361996-67-9
Molecular Formula:
Molecular Weight: 497.277
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: 4-methyl-N-(1,1,1-trifluoro-3-iodo-4-oxo-4-phenylbutan-2-yl)benzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: 4-methyl-N-(1,1,1-trifluoro-3-iodo-4-oxo-4-phenylbutan-2-yl)benzenesulfonamide(1361996-67-9)
EPA Substance Registry System: 4-methyl-N-(1,1,1-trifluoro-3-iodo-4-oxo-4-phenylbutan-2-yl)benzenesulfonamide(1361996-67-9)

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: 1361996-67-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1361996-67-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,1,9,9 and 6 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1361996-67:
(9*1)+(8*3)+(7*6)+(6*1)+(5*9)+(4*9)+(3*6)+(2*6)+(1*7)=199
199 % 10 = 9
So 1361996-67-9 is a valid CAS Registry Number.

1361996-67-9Upstream product

1361996-67-9Downstream Products

1361996-67-9Relevant academic research and scientific papers

Asymmetric iodoamination of chalcones and 4-aryl-4-oxobutenoates catalyzed by a complex based on scandium(III) and a N,N′-dioxide ligand

Cai, Yunfei,Liu, Xiaohua,Li, Jun,Chen, Weiliang,Wang, Wentao,Lin, Lili,Feng, Xiaoming

, p. 14916 - 14921 (2011)

Highly diastereo- and enantioselective iodoamination of chalcones, 4-aryl-4-oxobutenoates, and a trifluoro-substituted enone has been accomplished in the presence of a chiral N,N′-dioxide/[Sc(OTf)3] complex (0.5-2 mol%), delivering the desired

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