Cas 1290086-40-6,N-((S)-(4-chlorophenyl)-((R)-2,6-difluoro-1-oxo-2,3-dihydro-1H-inden-2yl)methyl)methanesulfonamide

1290086-40-6

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Basic information

Product Name: N-((S)-(4-chlorophenyl)-((R)-2,6-difluoro-1-oxo-2,3-dihydro-1H-inden-2yl)methyl)methanesulfonamide
Synonyms:
CAS NO:1290086-40-6
Molecular Formula:
Molecular Weight: 367.828
EINECS: N/A
Product Categories: N/A
Mol File: 1290086-40-6.mol
Article Data: 1

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-((S)-(4-chlorophenyl)-((R)-2,6-difluoro-1-oxo-2,3-dihydro-1H-inden-2yl)methyl)methanesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: N-((S)-(4-chlorophenyl)-((R)-2,6-difluoro-1-oxo-2,3-dihydro-1H-inden-2yl)methyl)methanesulfonamide(1290086-40-6)
EPA Substance Registry System: N-((S)-(4-chlorophenyl)-((R)-2,6-difluoro-1-oxo-2,3-dihydro-1H-inden-2yl)methyl)methanesulfonamide(1290086-40-6)

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: 1290086-40-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1290086-40-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,9,0,0,8 and 6 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1290086-40:
(9*1)+(8*2)+(7*9)+(6*0)+(5*0)+(4*8)+(3*6)+(2*4)+(1*0)=146
146 % 10 = 6
So 1290086-40-6 is a valid CAS Registry Number.

1290086-40-6Upstream product

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1290086-40-6Relevant articles and documents

Fluorinated aromatic ketones as nucleophiles in the asymmetric organocatalytic formation of C-C and C-N bonds: A facile route to the construction of fluorinated quaternary stereogenic centers

Zhao, Yujun,Pan, Yuanhang,Liu, Hongjun,Yang, Yuanyong,Jiang, Zhiyong,Tan, Choon-Hong

, p. 3571 - 3574 (2011/05/05)

Highly enantioselective Mannich and α-amination reactions have been successfully developed using α-fluorinated aromatic ketones as fluorocarbon nucleophiles in the presence of a bicyclic chiral guanidine (see scheme; Ms=methanesulfonyl). This method is a

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