106750-89-4 Usage
Chemical structure
A synthetic organic compound with two chloromethyl groups attached to a dihydro-ethanoanthracene backbone.
Synonyms
ICR 191
Application
Used as a building block in the chemical industry for the synthesis of various organic compounds, such as dyes, pigments, and pharmaceuticals.
Reactivity
The chloromethyl groups are reactive and can be used as a site for further chemical modification.
Toxicity
The compound may exhibit toxic properties and should be handled with care.
Flammability
The compound may be flammable, requiring caution during handling and storage.
Safety precautions
Should be handled in a controlled laboratory setting to minimize risks associated with its toxic and flammable properties.
Environmental and health concerns
Due to potential environmental and health risks, the use and production of ICR 191 may be regulated.
Regulatory considerations
Compliance with relevant safety and environmental regulations is necessary when working with ICR 191.
Storage
Proper storage conditions, such as in a cool, dry, and well-ventilated area, away from ignition sources, should be maintained to ensure the safety of the compound.
Disposal
Safe and responsible disposal methods should be followed to minimize the environmental impact of ICR 191.
Check Digit Verification of cas no
The CAS Registry Mumber 106750-89-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,7,5 and 0 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 106750-89:
(8*1)+(7*0)+(6*6)+(5*7)+(4*5)+(3*0)+(2*8)+(1*9)=124
124 % 10 = 4
So 106750-89-4 is a valid CAS Registry Number.
106750-89-4Relevant academic research and scientific papers
A CONVENIENT SYNTHESIS OF 2-AZATRIPTYCENE USING METHYLENEIMINE HYDROCHLORIDE
Skvarchenko, V. R.,Lapteva, V. L.,Gorbunova, M. A.
, p. 2244 - 2245 (2007/10/02)
A convenient method was developed for the production of 2-azatriptycene by the diene synthesis with methyleneimine hydrochloride and 11,12-dimethylene-9,10-dihydro-9,10-ethanoanthracene followed by thermal transformation of the obtained adduct.
IPTYCENES EXTENDED TRIPTYCENES
Hart, Harold,Bashir-Hashemi, Abdollah,Luo, Jihmei,Meador, Mary Ann
, p. 1641 - 1654 (2007/10/02)
Triptycene is the first member of a large scale of compounds for which we have coined the general term "iptycenes".The prefix (tri, pent, etc.) indicates the number of separated arene planes.By fusing from one to six 9,10-anthradiyl moieties on the triptycene framework, one can derive a first generation of iptycenes (Table 1).Of these, only 3, 4, 8 and a substituted 2 are known; the remainder provide a synthetic challenge.Potentially interesting practical and theorethical properties of iptycenes and particular structural features of several (i.e. 15, 16 and 24) arebriefly discussed, as are certain extensions beyond the compounds in Table 1.Methods for preparing useful synthons 35-41 are described.Three new, much improved syntheses of triptycene 29, itself a useful iptycene synthon, are presented.In addition, improved syntheses of pentiptycenes 3 and 33 are described, as well as the first syntheses of pentiptycenes 32, 34 and 52 and heptiptycene 54.The way is paved for future development of this mini-domain of unnatural products.
