7073-93-0 Usage
Description
m-Chlorocumene, with the molecular formula C9H11Cl, is a colorless liquid characterized by a pungent odor. It is a versatile chemical compound known for its use as a fragrance and flavoring agent, as well as in the production of pharmaceuticals, agrochemicals, and other fine chemicals. Although considered relatively stable and non-reactive under normal conditions, m-chlorocumene is classified as a hazardous material and requires careful handling to prevent eye and skin irritation.
Uses
Used in Fragrance and Flavoring Industry:
m-Chlorocumene is utilized as a fragrance and flavoring agent due to its distinctive aromatic properties. It imparts a unique scent and taste to various products, enhancing their appeal to consumers.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, m-chlorocumene serves as a key intermediate in the synthesis of various drugs. Its chemical structure allows for the development of new medications with potential therapeutic benefits.
Used in Agrochemical Industry:
m-Chlorocumene is also employed in the production of agrochemicals, contributing to the development of effective pesticides and other agricultural products that protect crops and enhance yield.
Used in Fine Chemicals Industry:
This versatile compound is further used in the synthesis of fine chemicals, which are essential in a wide range of applications, including the manufacture of dyes, plastics, and other specialty chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 7073-93-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,7 and 3 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7073-93:
(6*7)+(5*0)+(4*7)+(3*3)+(2*9)+(1*3)=100
100 % 10 = 0
So 7073-93-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H11Cl/c1-7(2)8-4-3-5-9(10)6-8/h3-7H,1-2H3
7073-93-0Relevant articles and documents
Murahashi Cross-Coupling at ?78 °C: A One-Pot Procedure for Sequential C?C/C?C, C?C/C?N, and C?C/C?S Cross-Coupling of Bromo-Chloro-Arenes
Sinha, Narayan,Heijnen, Dorus,Feringa, Ben L.,Organ, Michael G.
supporting information, p. 9180 - 9184 (2019/07/04)
The coupling of organolithium reagents, including strongly hindered examples, at cryogenic temperatures (as low as ?78 °C) has been achieved with high-reactivity Pd-NHC catalysts. A temperature-dependent chemoselectivity trigger has been developed for the selective coupling of aryl bromides in the presence of chlorides. Building on this, a one-pot, sequential coupling strategy is presented for the rapid construction of advanced building blocks. Importantly, one-shot addition of alkyllithium compounds to Pd cross-coupling reactions has been achieved, eliminating the need for slow addition by syringe pump.
PROCESS FOR HALOGENATION OF BENZENE AND BENZENE DERIVATIVES
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Page/Page column 18; 19, (2008/06/13)
In a process of halogenation of benzene or benzene derivatives, di-substituted halobenzene derivatives having para-aromatic compounds or tri-substituted halobenzene derivatives having 1,2,4-substituted aromatic compounds are selectively produced. In halogenation of benzene or benzene derivatives, a fluorine-containing zeolite catalyst such as L-type zeolite, or a zeolite catalyst having the crystal size of at most 100 nm is used. The reaction is preferably effected in the presence of a solvent, and the solvent is preferably a halogenated compound.
Direct Geminal Dimethylation of Aromatic Aldehydes with Dichlorodimethyltitanium
Reetz, Manfred T.,Kyung, Suk-Hun
, p. 123 - 124 (2007/10/02)
Aromatic aldehydes react specifically with (CH3)2TiCl2 to form the geminal dimethylated products.
