Cas 1127943-34-3,(3-bromo-2-[(trimethylsilyl)oxy]-5-{2-[(trimethylsilyl)oxy]ethyl}phenyl)(trimethyl)silane

1127943-34-3

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Basic information

Product Name: (3-bromo-2-[(trimethylsilyl)oxy]-5-{2-[(trimethylsilyl)oxy]ethyl}phenyl)(trimethyl)silane
Synonyms: (3-bromo-2-[(trimethylsilyl)oxy]-5-{2-[(trimethylsilyl)oxy]ethyl}phenyl)(trimethyl)silane
CAS NO:1127943-34-3
Molecular Formula:
Molecular Weight: 433.608
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: (3-bromo-2-[(trimethylsilyl)oxy]-5-{2-[(trimethylsilyl)oxy]ethyl}phenyl)(trimethyl)silane(CAS DataBase Reference)
NIST Chemistry Reference: (3-bromo-2-[(trimethylsilyl)oxy]-5-{2-[(trimethylsilyl)oxy]ethyl}phenyl)(trimethyl)silane(1127943-34-3)
EPA Substance Registry System: (3-bromo-2-[(trimethylsilyl)oxy]-5-{2-[(trimethylsilyl)oxy]ethyl}phenyl)(trimethyl)silane(1127943-34-3)

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: 1127943-34-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1127943-34-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,2,7,9,4 and 3 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1127943-34:
(9*1)+(8*1)+(7*2)+(6*7)+(5*9)+(4*4)+(3*3)+(2*3)+(1*4)=153
153 % 10 = 3
So 1127943-34-3 is a valid CAS Registry Number.

1127943-34-3Upstream product

75-77-4 chloro-trimethyl-silane

1127943-34-3Downstream Products

1127943-68-3 N-{2-[3-bromo-4-hydroxy-5-(trimethylsilyl)phenyl]ethyl}-N-methyl-4-nitrobenzenesulfonamide

1127943-34-3Relevant academic research and scientific papers

Oxidative Friedel-Crafts reaction and its application to the total syntheses of Amaryllidaceae alkaloids

Guerard, Kimiaka C.,Sabot, Cyrille,Racicot, Leanne,Canesi, Sylvain

supporting information; experimental part, p. 2039 - 2045 (2009/07/01)

An oxidative Friedel-Crafts reaction involving different aromatic compounds mediated by a hypervalent iodine reagent has been performed, using polysubstituted phenols. The strategy fits within the concept of "aromatic ring umpolung", which opens up novel

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