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Details

Stereochemistry ACHIRAL
Molecular Formula C7H7NO2
Molecular Weight 137.136
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PHENYL CARBAMATE

SMILES

NC(=O)OC1=CC=CC=C1

InChI

InChIKey=BSCCSDNZEIHXOK-UHFFFAOYSA-N
InChI=1S/C7H7NO2/c8-7(9)10-6-4-2-1-3-5-6/h1-5H,(H2,8,9)

HIDE SMILES / InChI

Molecular Formula C7H7NO2
Molecular Weight 137.136
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Targeted intracellular delivery of antisense oligonucleotides via conjugation with small-molecule ligands.
2010-07-07
Biodegradable calcium phosphate nanoparticle with lipid coating for systemic siRNA delivery.
2010-03-19
Preparation and characterization of laminin-derived peptide AG73-coated liposomes as a selective gene delivery tool.
2010
Novel estrogen receptor (ER) modulators: carbamate and thiocarbamate derivatives with m-carborane bisphenol structure.
2009-12-01
Electrophoretically mediated microanalysis technique as a tool for the rapid screening of novel acetylcholinesterase inhibitors.
2009-08-26
Novel cationic lipid that delivers siRNA and enhances therapeutic effect in lung cancer cells.
2009-03-10
Sulfated and sulfonated polysaccharide as chiral stationary phases for capillary electrochromatography and capillary electrochromatography-mass spectrometry.
2009-01-30
2-Isopropoxyphenyl N-methyl-carbamate.
2009-01-23
Asymmetric synthesis of the ABC-ring system of the antitumor antibiotic MPC1001.
2009-01-16
An efficient and low immunostimulatory nanoparticle formulation for systemic siRNA delivery to the tumor.
2008-10-06
Efficient oncogene silencing and metastasis inhibition via systemic delivery of siRNA.
2008-05
Efficient gene silencing in metastatic tumor by siRNA formulated in surface-modified nanoparticles.
2008-02-18
Tumor-targeted delivery of siRNA by self-assembled nanoparticles.
2008-01
Polymorphism and structural mechanism of the phase transformation of phenyl carbamate (PC).
2008
Carbanilation of cereal beta-glucans for molecular weight determination and conformational studies.
2007-08-13
High-affinity carbamate analogues of morphinan at opioid receptors.
2007-03-15
Targeted delivery of antisense oligodeoxynucleotide and small interference RNA into lung cancer cells.
2006-10-03
Determination of carbofuran, carbaryl and their main metabolites in plasma samples of agricultural populations using gas chromatography-tandem mass spectrometry.
2006-08
Anisamide-targeted stealth liposomes: a potent carrier for targeting doxorubicin to human prostate cancer cells.
2004-11-20
Enantiopure spiro[3.3]heptane-2,6-dicarboxylic acid.
2002-06-05
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:07:09 GMT 2025
Edited
by admin
on Mon Mar 31 18:07:09 GMT 2025
Record UNII
JKB257U27V
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-66509
Preferred Name English
PHENYL CARBAMATE
Systematic Name English
CARBAMIC ACID, PHENYL ESTER
Common Name English
Code System Code Type Description
NSC
66509
Created by admin on Mon Mar 31 18:07:09 GMT 2025 , Edited by admin on Mon Mar 31 18:07:09 GMT 2025
PRIMARY
ECHA (EC/EINECS)
210-737-1
Created by admin on Mon Mar 31 18:07:09 GMT 2025 , Edited by admin on Mon Mar 31 18:07:09 GMT 2025
PRIMARY
FDA UNII
JKB257U27V
Created by admin on Mon Mar 31 18:07:09 GMT 2025 , Edited by admin on Mon Mar 31 18:07:09 GMT 2025
PRIMARY
PUBCHEM
69322
Created by admin on Mon Mar 31 18:07:09 GMT 2025 , Edited by admin on Mon Mar 31 18:07:09 GMT 2025
PRIMARY
EPA CompTox
DTXSID20211237
Created by admin on Mon Mar 31 18:07:09 GMT 2025 , Edited by admin on Mon Mar 31 18:07:09 GMT 2025
PRIMARY
CAS
622-46-8
Created by admin on Mon Mar 31 18:07:09 GMT 2025 , Edited by admin on Mon Mar 31 18:07:09 GMT 2025
PRIMARY