Cas 110547-69-8,(4R,5R)-4-tert-Butyl-5-(4-chloro-phenyl)-3-methylene-2,2-bis-(2,4,6-trimethyl-phenyl)-[1,2]oxasilolane

110547-69-8

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Basic information

Product Name: (4R,5R)-4-tert-Butyl-5-(4-chloro-phenyl)-3-methylene-2,2-bis-(2,4,6-trimethyl-phenyl)-[1,2]oxasilolane
Synonyms:
CAS NO:110547-69-8
Molecular Formula:
Molecular Weight: 503.2
EINECS: N/A
Product Categories: N/A
Mol File: 110547-69-8.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: (4R,5R)-4-tert-Butyl-5-(4-chloro-phenyl)-3-methylene-2,2-bis-(2,4,6-trimethyl-phenyl)-[1,2]oxasilolane(CAS DataBase Reference)
NIST Chemistry Reference: (4R,5R)-4-tert-Butyl-5-(4-chloro-phenyl)-3-methylene-2,2-bis-(2,4,6-trimethyl-phenyl)-[1,2]oxasilolane(110547-69-8)
EPA Substance Registry System: (4R,5R)-4-tert-Butyl-5-(4-chloro-phenyl)-3-methylene-2,2-bis-(2,4,6-trimethyl-phenyl)-[1,2]oxasilolane(110547-69-8)

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: 110547-69-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 110547-69-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,5,4 and 7 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 110547-69:
(8*1)+(7*1)+(6*0)+(5*5)+(4*4)+(3*7)+(2*6)+(1*9)=98
98 % 10 = 8
So 110547-69-8 is a valid CAS Registry Number.

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110547-69-8Relevant articles and documents

REACTION OF SILYLENE WITH ALLENES: ALKYLIDENESILACYCLOPROPANE AND SILATRIMETHILENEMETANE

Ando, Wataru,Saso, Haruo

, p. 5625 - 5628 (1986)

Reaction of photogenerated dimethylsilylene with tert-butyldimethylallene and tert-butylallene yielded the corresponding alkylidenesilacyclopropanes.Its photochemical behavior and some reactions with nucleophiles are described.

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