Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C15H22N2O2 |
| Molecular Weight | 262.3474 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 4 / 4 |
| E/Z Centers | 2 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[H][C@]2(C[C@H]1CC[C@H](CC1)N=C=O)CC[C@@H](CC2)N=C=O
InChI
InChIKey=KORSJDCBLAPZEQ-JNCCQOAMSA-N
InChI=1S/C15H22N2O2/c18-10-16-14-5-1-12(2-6-14)9-13-3-7-15(8-4-13)17-11-19/h12-15H,1-9H2/t12-,13-,14-,15+
| Molecular Formula | C15H22N2O2 |
| Molecular Weight | 262.3474 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 4 / 4 |
| E/Z Centers | 2 |
| Optical Activity | UNSPECIFIED |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Use of hexyl isocyanate antigen to detect antibodies to hexamethylene diisocyanate (HDI) in sensitized guinea pigs and in a sensitized worker. | 1982 May-Jun |
|
| Characterization of murine immune responses to allergenic diisocyanates. | 1992 Feb |
|
| Variable effects of chemical allergens on serum IgE concentration in mice. Preliminary evaluation of a novel approach to the identification of respiratory sensitizers. | 1992 Oct |
|
| Phenyl isocyanate is a potent chemical sensitizer. | 1996 Dec 16 |
|
| Allergic contact dermatitis from dicyclohexylmethane-4,4'-diisocyanate. | 2003 Jun |
|
| Occupational allergic contact dermatitis in a company manufacturing boards coated with isocyanate lacquer. | 2003 May |
|
| Enzyme induced biodegradation of polycarbonate-polyurethanes: dose dependence effect of cholesterol esterase. | 2003 May |
|
| Acute inhalation studies with irritant aerosols: technical issues and relevance for risk characterization. | 2004 May |
|
| Cytokine mRNA profiles for isocyanates with known and unknown potential to induce respiratory sensitization. | 2005 Feb 28 |
|
| Histopathologic changes of porcine dermis xenografts for transvaginal suburethral slings. | 2005 May |
|
| Inconsistencies between cytokine profiles, antibody responses, and respiratory hyperresponsiveness following dermal exposure to isocyanates. | 2006 Nov |
|
| FTIR spectroscopic characterization of polyurethane-urea model hard segments (PUUMHS) based on three diamine chain extenders. | 2007 Jan |
|
| Preparation and surface characterization of HMDI-activated 316L stainless steel for coronary artery stents. | 2008 Jun 1 |
|
| Allergic contact dermatitis to DMDI in an office application. | 2008 May |
|
| Immobilization of NaIO4-treated heparin on PEG-modified 316L SS surface for high anti-thrombin-III binding. | 2008 Sep |
|
| Rapid development of allergic contact dermatitis from dicyclohexylmethane-4,4'-diisocyanate. | 2009 Jul-Aug |
|
| Synthesis of highly porous crosslinked elastin hydrogels and their interaction with fibroblasts in vitro. | 2009 Sep |
|
| A novel route to prepare Fe3O4/P(MAA-co-NVP) cross-linked magnetic composite microspheres with core-shell architecture by surface-initiated radical dispersion polymerization. | 2010 Dec |
|
| Degradation studies on segmented polyurethanes prepared with HMDI, PCL and different chain extenders. | 2010 Jun |
|
| [Synthesis and structure characterization of bis (4-butoxycarbonylaminocyclohexyl) methane]. | 2010 Sep |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 08:15:05 GMT 2023
by
admin
on
Sat Dec 16 08:15:05 GMT 2023
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| Record UNII |
6Y80AJA84R
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| Record Status |
Validated (UNII)
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| Record Version |
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Created by
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17901-48-3
Created by
admin on Sat Dec 16 08:15:05 GMT 2023 , Edited by admin on Sat Dec 16 08:15:05 GMT 2023
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PRIMARY |