Cas 934565-86-3,(R)-N-(3-iodo-4-methyl-phenyl)-4-methyl-N-1-oxiranylmethyl-benzenesulfonamide

934565-86-3

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Basic information

Product Name: (R)-N-(3-iodo-4-methyl-phenyl)-4-methyl-N-1-oxiranylmethyl-benzenesulfonamide
Synonyms: (R)-N-(3-iodo-4-methyl-phenyl)-4-methyl-N-1-oxiranylmethyl-benzenesulfonamide
CAS NO:934565-86-3
Molecular Formula:
Molecular Weight: 443.305
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: (R)-N-(3-iodo-4-methyl-phenyl)-4-methyl-N-1-oxiranylmethyl-benzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: (R)-N-(3-iodo-4-methyl-phenyl)-4-methyl-N-1-oxiranylmethyl-benzenesulfonamide(934565-86-3)
EPA Substance Registry System: (R)-N-(3-iodo-4-methyl-phenyl)-4-methyl-N-1-oxiranylmethyl-benzenesulfonamide(934565-86-3)

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: 934565-86-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 934565-86-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,4,5,6 and 5 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 934565-86:
(8*9)+(7*3)+(6*4)+(5*5)+(4*6)+(3*5)+(2*8)+(1*6)=203
203 % 10 = 3
So 934565-86-3 is a valid CAS Registry Number.

934565-86-3Upstream product

934565-86-3Downstream Products

934565-86-3Relevant academic research and scientific papers

Stereochemical and mechanistic investigations of a palladium-catalyzed annulation of secondary alkyl iodides

Rudolph, Alena,Rackelmann, Nils,Lautens, Mark

, p. 1485 - 1488 (2008/04/05)

(Chemical Equation Presented) Inversion versus retention: A palladium-catalyzed annulation with enantioenriched secondary alkyl iodides gives mechanistic insight into the stereochemistry of this C-H bond functionalization reaction (see scheme) involving a

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