Cas 160422-47-9,N-<2-(2-iodo-4,5-dimethoxyphenyl)ethyl>-N-<4-(trimethylsilyl)but-2-ynyl>mesitylenesulfonamide

160422-47-9

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Basic information

Product Name: N-<2-(2-iodo-4,5-dimethoxyphenyl)ethyl>-N-<4-(trimethylsilyl)but-2-ynyl>mesitylenesulfonamide
Synonyms: N-<2-(2-iodo-4,5-dimethoxyphenyl)ethyl>-N-<4-(trimethylsilyl)but-2-ynyl>mesitylenesulfonamide
CAS NO:160422-47-9
Molecular Formula:
Molecular Weight: 613.632
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-<2-(2-iodo-4,5-dimethoxyphenyl)ethyl>-N-<4-(trimethylsilyl)but-2-ynyl>mesitylenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: N-<2-(2-iodo-4,5-dimethoxyphenyl)ethyl>-N-<4-(trimethylsilyl)but-2-ynyl>mesitylenesulfonamide(160422-47-9)
EPA Substance Registry System: N-<2-(2-iodo-4,5-dimethoxyphenyl)ethyl>-N-<4-(trimethylsilyl)but-2-ynyl>mesitylenesulfonamide(160422-47-9)

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: 160422-47-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 160422-47-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,4,2 and 2 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 160422-47:
(8*1)+(7*6)+(6*0)+(5*4)+(4*2)+(3*2)+(2*4)+(1*7)=99
99 % 10 = 9
So 160422-47-9 is a valid CAS Registry Number.

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160422-47-9Relevant academic research and scientific papers

Stereoselective Synthesis of Exocyclic Allylsilanes by Intramolecular Reductive Heck Cyclisation of Propargylsilanes

Tietze, Lutz F.,Schimpf, Ralph

, p. 2235 - 2240 (2007/10/02)

The stereoselective palladium-catalysed synthesis of the heterocycles 13-15 with a (Z)-exocyclic allylsilane moiety is described.Alkylation of the secondary amides 5a, 5b, 9a, and 9b and the phenol 11 containing an iodoaryl moiety with the propargyl iodid

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