Cas 849024-99-3,Benzenesulfonamide, N-[[[(1R,2R)-2-(dimethylamino)cyclohexyl]amino]carbonyl]-4-methyl-

849024-99-3

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Basic information

Product Name: Benzenesulfonamide, N-[[[(1R,2R)-2-(dimethylamino)cyclohexyl]amino]carbonyl]-4-methyl-
Synonyms:
CAS NO:849024-99-3
Molecular Formula: C16H25N3O3S
Molecular Weight: 339.459
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: Benzenesulfonamide, N-[[[(1R,2R)-2-(dimethylamino)cyclohexyl]amino]carbonyl]-4-methyl-(CAS DataBase Reference)
NIST Chemistry Reference: Benzenesulfonamide, N-[[[(1R,2R)-2-(dimethylamino)cyclohexyl]amino]carbonyl]-4-methyl-(849024-99-3)
EPA Substance Registry System: Benzenesulfonamide, N-[[[(1R,2R)-2-(dimethylamino)cyclohexyl]amino]carbonyl]-4-methyl-(849024-99-3)

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: 849024-99-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 849024-99-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,9,0,2 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 849024-99:
(8*8)+(7*4)+(6*9)+(5*0)+(4*2)+(3*4)+(2*9)+(1*9)=193
193 % 10 = 3
So 849024-99-3 is a valid CAS Registry Number.

849024-99-3Upstream product

849024-99-3Downstream Products

849024-99-3Relevant academic research and scientific papers

Enantio- and diastereoselective addition of thioacetic acid to nitroalkenes via N-sulfinyl urea catalysis

Kimmel, Kyle L.,Robak, Maryann T.,Thomas, Stephen,Lee, Melissa,Ellman, Jonathan A.

, p. 2704 - 2712 (2012)

The enantioselective addition of thioacetic acid to nitroalkenes was achieved using N-sulfinyl urea catalysis. In this report, the scope of the reaction was extended to the enantio- and diastereoselective thioacetic acid addition to cyclic α,β-disubstitut

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