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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
Structure of 4,4'-DIISOCYANATODICYCLOHEXYLMETHANE, CIS,CIS-

SMILES

O=C=N[C@@H]1CC[C@H](C[C@H]2CC[C@H](CC2)N=C=O)CC1

InChI

InChIKey=KORSJDCBLAPZEQ-VLRMEEEOSA-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+

HIDE SMILES / InChI

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

PubMed

TitleDatePubMed
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.
2010-12
[Synthesis and structure characterization of bis (4-butoxycarbonylaminocyclohexyl) methane].
2010-09
Degradation studies on segmented polyurethanes prepared with HMDI, PCL and different chain extenders.
2010-06
Rapid development of allergic contact dermatitis from dicyclohexylmethane-4,4'-diisocyanate.
2009-10-07
Synthesis of highly porous crosslinked elastin hydrogels and their interaction with fibroblasts in vitro.
2009-09
Immobilization of NaIO4-treated heparin on PEG-modified 316L SS surface for high anti-thrombin-III binding.
2008-09
Preparation and surface characterization of HMDI-activated 316L stainless steel for coronary artery stents.
2008-06-01
Allergic contact dermatitis to DMDI in an office application.
2008-05
FTIR spectroscopic characterization of polyurethane-urea model hard segments (PUUMHS) based on three diamine chain extenders.
2007-01
Inconsistencies between cytokine profiles, antibody responses, and respiratory hyperresponsiveness following dermal exposure to isocyanates.
2006-11
Histopathologic changes of porcine dermis xenografts for transvaginal suburethral slings.
2005-05
Cytokine mRNA profiles for isocyanates with known and unknown potential to induce respiratory sensitization.
2005-02-28
Acute inhalation studies with irritant aerosols: technical issues and relevance for risk characterization.
2004-05
Allergic contact dermatitis from dicyclohexylmethane-4,4'-diisocyanate.
2003-06
Occupational allergic contact dermatitis in a company manufacturing boards coated with isocyanate lacquer.
2003-05
Enzyme induced biodegradation of polycarbonate-polyurethanes: dose dependence effect of cholesterol esterase.
2003-05
Phenyl isocyanate is a potent chemical sensitizer.
1996-12-16
Variable effects of chemical allergens on serum IgE concentration in mice. Preliminary evaluation of a novel approach to the identification of respiratory sensitizers.
1992-10
Characterization of murine immune responses to allergenic diisocyanates.
1992-02
Use of hexyl isocyanate antigen to detect antibodies to hexamethylene diisocyanate (HDI) in sensitized guinea pigs and in a sensitized worker.
1982-05-01
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:05:03 GMT 2025
Edited
by admin
on Mon Mar 31 22:05:03 GMT 2025
Record UNII
P815VNF99I
Record Status Validated (UNII)
Record Version
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Name Type Language
CIS,CIS-4,4'-DIISOCYANATODICYCLOHEXYLMETHANE
Preferred Name English
4,4'-DIISOCYANATODICYCLOHEXYLMETHANE, CIS,CIS-
Common Name English
CYCLOHEXANE, 1,1'-METHYLENEBIS(4-ISOCYANATO-, (CIS(CIS))-
Systematic Name English
CIS-CIS-METHYLENE BIS(4-CYCLOHEXYLISOCYANATE)
Common Name English
ISOCYANIC ACID, METHYLENEDI-4,1-CYCLOHEXYLENE ESTER, CIS,CIS-
Systematic Name English
Code System Code Type Description
CAS
18937-00-3
Created by admin on Mon Mar 31 22:05:03 GMT 2025 , Edited by admin on Mon Mar 31 22:05:03 GMT 2025
PRIMARY
FDA UNII
P815VNF99I
Created by admin on Mon Mar 31 22:05:03 GMT 2025 , Edited by admin on Mon Mar 31 22:05:03 GMT 2025
PRIMARY