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Details

Stereochemistry ACHIRAL
Molecular Formula C13H22N2
Molecular Weight 206.3272
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 2
Charge 0

SHOW SMILES / InChI
Structure of DICYCLOHEXYLCARBODIIMIDE

SMILES

C1CCC(CC1)N=C=NC2CCCCC2

InChI

InChIKey=QOSSAOTZNIDXMA-UHFFFAOYSA-N
InChI=1S/C13H22N2/c1-3-7-12(8-4-1)14-11-15-13-9-5-2-6-10-13/h12-13H,1-10H2

HIDE SMILES / InChI

Molecular Formula C13H22N2
Molecular Weight 206.3272
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 2
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
The effect of amino acid-modifying reagents on chloroplast protein import and the formation of early import intermediates.
2001 Jan
A simple synthetic route to the formation of a block copolymer of poly(lactic-co-glycolic acid) and polylysine for the fabrication of functionalized, degradable structures for biomedical applications.
2001 May 1
H+-ATPase defect in Corynebacterium glutamicum abolishes glutamic acid production with enhancement of glucose consumption rate.
2001 Nov
[Comparative study of inhibiting photophosphorylation and light-activated ATP hydrolysis in pea chloroplasts by N,N'-dicyclohexylcarbodiimide].
2001 Sep-Oct
[ATPase activity of Neisseria gonorrhoeae and Staphylococcus aureus strains].
2001 Sep-Oct
ATP generation during reduced inorganic sulfur compound oxidation by Acidithiobacillus caldus is exclusively due to electron transport phosphorylation.
2002 Apr
Sulfite inhibits the F1F0-ATP synthase and activates the F1F0-ATPase of Paracoccus denitrificans.
2002 Aug
Synthesis and biological evaluation of N-substituted indole esters as inhibitors of cyclo-oxygenase-2 (COX-2).
2002 Aug
Synthesis of feralex a novel aluminum/iron chelating compound.
2002 Jan 1
Building blocks for the solution phase synthesis of oligonucleotides: regioselective hydrolysis of 3',5'-Di-O-levulinylnucleosides using an enzymatic approach.
2002 Jun 28
Genetic fusions of globular proteins to the epsilon subunit of the Escherichia coli ATP synthase: Implications for in vivo rotational catalysis and epsilon subunit function.
2002 May 10
Membrane embedded location of Na+ or H+ binding sites on the rotor ring of F1F0 ATP synthases.
2002 Nov
MHC restriction in contact hypersensitivity to dicyclohexylcarbodiimide.
2002 Nov
Zinc biosorption from aqueous solution by a halotolerant cyanobacterium Aphanothece halophytica.
2002 Oct
Acute stress modulates the irritant component of sensitizers in allergic contact dermatitis: implications for exposure assessment.
2003 Apr 1
Identification of organelles in bacteria similar to acidocalcisomes of unicellular eukaryotes.
2003 Aug 8
Evidence for structural integrity in the undecameric c-rings isolated from sodium ATP synthases.
2003 Jan 10
Traceless liquid phase synthesis of piperazinediones.
2003 Mar
Immobilization of D-ribulose-1,5-bisphosphate carboxylase/oxygenase: a step toward carbon dioxide fixation bioprocess.
2003 Mar 20
[Changes in hydrodynamic diameter of myometrium plasmalemma vesicles under artificial creation of transmembrane proton gradients].
2003 Mar-Apr
Mode of action of pyrazinamide: disruption of Mycobacterium tuberculosis membrane transport and energetics by pyrazinoic acid.
2003 Nov
Inhibition studies on Rhodospirillum rubrum H(+)-pyrophosphatase expressed in Escherichia coli.
2004 Jun 7
Self-assembled polymeric nanoparticles of poly(ethylene glycol) grafted pullulan acetate as a novel drug carrier.
2004 May
Reversible assembly of the ATP-binding cassette transporter Mdl1 with the F1F0-ATP synthase in mitochondria.
2004 Sep 10
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 14:59:00 GMT 2023
Edited
by admin
on Fri Dec 15 14:59:00 GMT 2023
Record UNII
0T1427205E
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DICYCLOHEXYLCARBODIIMIDE
HSDB   MI  
Systematic Name English
CYCLOHEXANAMINE, N,N'-METHANETETRAYLBIS-
Common Name English
NSC-53373
Code English
NSC-57182
Code English
N,N'-DICYCLOHEXYLCARBODIIMIDE
Systematic Name English
DCC
Common Name English
DICYCLOHEXYLCARBODIIMIDE [HSDB]
Common Name English
DICYCLOHEXYLCARBODIIMIDE [MI]
Common Name English
NSC-30022
Code English
DICYCLOHEXYL-CARBODIIMIDE
Systematic Name English
Code System Code Type Description
NSC
53373
Created by admin on Fri Dec 15 14:59:00 GMT 2023 , Edited by admin on Fri Dec 15 14:59:00 GMT 2023
PRIMARY
NSC
57182
Created by admin on Fri Dec 15 14:59:00 GMT 2023 , Edited by admin on Fri Dec 15 14:59:00 GMT 2023
PRIMARY
CAS
538-75-0
Created by admin on Fri Dec 15 14:59:00 GMT 2023 , Edited by admin on Fri Dec 15 14:59:00 GMT 2023
PRIMARY
PUBCHEM
10868
Created by admin on Fri Dec 15 14:59:00 GMT 2023 , Edited by admin on Fri Dec 15 14:59:00 GMT 2023
PRIMARY
MERCK INDEX
m4377
Created by admin on Fri Dec 15 14:59:00 GMT 2023 , Edited by admin on Fri Dec 15 14:59:00 GMT 2023
PRIMARY Merck Index
CHEBI
53090
Created by admin on Fri Dec 15 14:59:00 GMT 2023 , Edited by admin on Fri Dec 15 14:59:00 GMT 2023
PRIMARY
NSC
30022
Created by admin on Fri Dec 15 14:59:00 GMT 2023 , Edited by admin on Fri Dec 15 14:59:00 GMT 2023
PRIMARY
EPA CompTox
DTXSID1023817
Created by admin on Fri Dec 15 14:59:00 GMT 2023 , Edited by admin on Fri Dec 15 14:59:00 GMT 2023
PRIMARY
ECHA (EC/EINECS)
208-704-1
Created by admin on Fri Dec 15 14:59:00 GMT 2023 , Edited by admin on Fri Dec 15 14:59:00 GMT 2023
PRIMARY
HSDB
8049
Created by admin on Fri Dec 15 14:59:00 GMT 2023 , Edited by admin on Fri Dec 15 14:59:00 GMT 2023
PRIMARY
FDA UNII
0T1427205E
Created by admin on Fri Dec 15 14:59:00 GMT 2023 , Edited by admin on Fri Dec 15 14:59:00 GMT 2023
PRIMARY
WIKIPEDIA
Dicyclohexylcarbodiimide
Created by admin on Fri Dec 15 14:59:00 GMT 2023 , Edited by admin on Fri Dec 15 14:59:00 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> IMPURITY