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
Rapid homogeneous lauroylation of wheat straw hemicelluloses under mild conditions.
2008-11-24
Studies of the lauroylation of wheat straw hemicelluloses under heating.
2008-02-27
An easy synthetic approach to pyridoporphyrins by domino reactions.
2007-06-07
Photophysical properties of luminescent quaternary lanthanide molecular hybrid systems with chemical bonds from the cooperative design and assembly of structure and function.
2007-03
Inhibition of influenza-virus-induced cytopathy by sialylglycoconjugates.
2006-09-25
Surface esterification of cellulose fibers: characterization by DRIFT and contact angle measurements.
2006-03-01
Synthesis of lipophilic poly-lauroyl-(+)-catechins and radical-scavenging activity.
2005-03
Chemical valorization of forest and agricultural by-products. Obtention, chemical characteristics, and mechanical behavior of a novel family of hydrophobic films.
2004-05
Engineering of dendrimer surfaces to enhance transepithelial transport and reduce cytotoxicity.
2003-10
Patents
Name Type Language
DODECANOYL CHLORIDE
HSDB  
Preferred Name English
LAUROYL CHLORIDE
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 Mon Mar 31 22:18:54 GMT 2025 , Edited by admin on Mon Mar 31 22:18:54 GMT 2025
PRIMARY
EPA CompTox
DTXSID5044368
Created by admin on Mon Mar 31 22:18:54 GMT 2025 , Edited by admin on Mon Mar 31 22:18:54 GMT 2025
PRIMARY
HSDB
5567
Created by admin on Mon Mar 31 22:18:54 GMT 2025 , Edited by admin on Mon Mar 31 22:18:54 GMT 2025
PRIMARY
FDA UNII
9LHL10777I
Created by admin on Mon Mar 31 22:18:54 GMT 2025 , Edited by admin on Mon Mar 31 22:18:54 GMT 2025
PRIMARY
DRUG BANK
DB14670
Created by admin on Mon Mar 31 22:18:54 GMT 2025 , Edited by admin on Mon Mar 31 22:18:54 GMT 2025
PRIMARY
CAS
112-16-3
Created by admin on Mon Mar 31 22:18:54 GMT 2025 , Edited by admin on Mon Mar 31 22:18:54 GMT 2025
PRIMARY
ECHA (EC/EINECS)
203-941-7
Created by admin on Mon Mar 31 22:18:54 GMT 2025 , Edited by admin on Mon Mar 31 22:18:54 GMT 2025
PRIMARY