32223-70-4 Usage
General Description
4-(hexyloxy)phenyl isocyanate is a chemical compound that belongs to the class of isocyanate compounds, which are known to be potent sensitizers and irritants. It is used in various industries, including the production of adhesives, sealants, and coatings. This chemical can cause skin and respiratory irritation, and long-term exposure has been associated with respiratory sensitization and asthma. Additionally, 4-(hexyloxy)phenyl isocyanate is considered to be a potential human carcinogen, and precautions should be taken to minimize exposure and prevent adverse health effects.
Check Digit Verification of cas no
The CAS Registry Mumber 32223-70-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,2,2 and 3 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 32223-70:
(7*3)+(6*2)+(5*2)+(4*2)+(3*3)+(2*7)+(1*0)=74
74 % 10 = 4
So 32223-70-4 is a valid CAS Registry Number.
InChI:InChI=1/C13H17NO2/c1-2-3-4-5-10-16-13-8-6-12(7-9-13)14-11-15/h6-9H,2-5,10H2,1H3
32223-70-4Relevant articles and documents
Oxime Carbamate-Discovery of a series of novel FAAH inhibitors
Sit,Conway, Charles M.,Xie, Kai,Bertekap, Robert,Bourin, Clotilde,Burris, Kevin D.
supporting information; experimental part, p. 1272 - 1277 (2010/06/17)
A series of novel oxime carbamates have been identified as potent inhibitors of the key regulatory enzyme of the endocannabinoid signaling system, fatty acid amide hydrolase (FAAH). In this Letter, the rationale behind the discovery and the biological evaluations of this novel class of FAAH inhibitors are presented. Both in vitro and in vivo results of selected targets are discussed, along with inhibition kinetics and molecular modeling studies.1.
Anthelmintic 1-(substituted phenyl)-3-alkanimidoyl ureas
-
, (2008/06/13)
The compounds of this invention are novel imidoylureas having anthelmintic activity and imidoylthioureas having antifertility activity. They are prepared by the reaction of appropriate amidines with appropriate isocyanates or isothiocyanates.
