U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C12H23ClO
Molecular Weight 218.763
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LAUROYL CHLORIDE

SMILES

CCCCCCCCCCCC(Cl)=O

InChI

InChIKey=NQGIJDNPUZEBRU-UHFFFAOYSA-N
InChI=1S/C12H23ClO/c1-2-3-4-5-6-7-8-9-10-11-12(13)14/h2-11H2,1H3

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Engineering of dendrimer surfaces to enhance transepithelial transport and reduce cytotoxicity.
2003 Oct
Chemical valorization of forest and agricultural by-products. Obtention, chemical characteristics, and mechanical behavior of a novel family of hydrophobic films.
2004 May
Synthesis of lipophilic poly-lauroyl-(+)-catechins and radical-scavenging activity.
2005 Mar
Surface esterification of cellulose fibers: characterization by DRIFT and contact angle measurements.
2006 Mar 1
Inhibition of influenza-virus-induced cytopathy by sialylglycoconjugates.
2006 Sep 25
An easy synthetic approach to pyridoporphyrins by domino reactions.
2007 Jun 7
Photophysical properties of luminescent quaternary lanthanide molecular hybrid systems with chemical bonds from the cooperative design and assembly of structure and function.
2007 Mar
Studies of the lauroylation of wheat straw hemicelluloses under heating.
2008 Feb 27
Rapid homogeneous lauroylation of wheat straw hemicelluloses under mild conditions.
2008 Nov 24
Patents
Name Type Language
LAUROYL CHLORIDE
Systematic Name English
DODECANOYL CHLORIDE
HSDB  
Systematic Name English
N-DODECANOYL CHLORIDE
Common Name English
DODECANOIC ACID, CHLORIDE
Systematic Name English
DODECANOYL CHLORIDE [HSDB]
Common Name English
LAURIC ACID CHLORIDE
Systematic Name English
Code System Code Type Description
PUBCHEM
8166
Created by admin on Sat Dec 16 08:47:22 GMT 2023 , Edited by admin on Sat Dec 16 08:47:22 GMT 2023
PRIMARY
EPA CompTox
DTXSID5044368
Created by admin on Sat Dec 16 08:47:22 GMT 2023 , Edited by admin on Sat Dec 16 08:47:22 GMT 2023
PRIMARY
HSDB
5567
Created by admin on Sat Dec 16 08:47:22 GMT 2023 , Edited by admin on Sat Dec 16 08:47:22 GMT 2023
PRIMARY
FDA UNII
9LHL10777I
Created by admin on Sat Dec 16 08:47:22 GMT 2023 , Edited by admin on Sat Dec 16 08:47:22 GMT 2023
PRIMARY
DRUG BANK
DB14670
Created by admin on Sat Dec 16 08:47:22 GMT 2023 , Edited by admin on Sat Dec 16 08:47:22 GMT 2023
PRIMARY
CAS
112-16-3
Created by admin on Sat Dec 16 08:47:22 GMT 2023 , Edited by admin on Sat Dec 16 08:47:22 GMT 2023
PRIMARY
ECHA (EC/EINECS)
203-941-7
Created by admin on Sat Dec 16 08:47:22 GMT 2023 , Edited by admin on Sat Dec 16 08:47:22 GMT 2023
PRIMARY