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

Details

Stereochemistry ACHIRAL
Molecular Formula C8H10O2
Molecular Weight 138.1638
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 1,4-DIMETHOXYBENZENE

SMILES

COC1=CC=C(OC)C=C1

InChI

InChIKey=OHBQPCCCRFSCAX-UHFFFAOYSA-N
InChI=1S/C8H10O2/c1-9-7-3-5-8(10-2)6-4-7/h3-6H,1-2H3

HIDE SMILES / InChI

Molecular Formula C8H10O2
Molecular Weight 138.1638
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Reactions of N-methyl-N-(4-biphenylyl)nitrenium ion with electron-rich arenes: laser flash photolysis and product studies.
2002 Apr 10
One-pot synthesis of C-glycosylic compounds (C-glycosides) from D-glucal, p-tolylsulfenyl chloride and aromatic/heteroaromatic compounds in the presence of Lewis acids.
2002 Aug 16
Atomic structures of human dihydrofolate reductase complexed with NADPH and two lipophilic antifolates at 1.09 a and 1.05 a resolution.
2002 Jul 12
Bridge-mediated hopping or superexchange electron-transfer processes in bis(triarylamine) systems.
2002 Sep
Dendrimers as ligands. Formation of a 2:1 luminescent complex between a dendrimer with a 1,4,8,11-tetraazacyclotetradecane (cyclam) core and Zn2+.
2003 Apr 16
Efficient synthesis of porphyrin-containing, benzoquinone-terminated, rigid polyphenylene dendrimers.
2003 Jan 24
Synthesis of biotinylated xestoquinone that retains inhibitory activity against Ca2+ ATPase of skeletal muscle myosin.
2003 Jul 17
Guest-induced assembly of tetracarboxyl-cavitand and tetra(3-pyridyl)-cavitand into a heterodimeric capsule via hydrogen bonds and CH-halogen and/or CH-pi interaction: control of the orientation of the encapsulated guest.
2003 Sep 3
Analysis of biogenic volatile organic compounds in zucchini flowers: identification of scent sources.
2005 Oct
Effect of water on the functionalization of substituted anisoles with iodine in the presence of F-TEDA-BF4 or hydrogen peroxide.
2006 Feb 3
Selective monoiodination of aromatic compounds with electrochemically generated I+ using micromixing.
2006 Sep 28
Structure-activity relationship studies on a novel class of antiproliferative agents derived from Lavendustin A. Part I: Ring A modifications.
2008 Aug 15
Application of microscale-preparative multidimensional gas chromatography with nuclear magnetic resonance spectroscopy for identification of pure methylnaphthalenes from crude oils.
2008 Dec 26
1,4-Di-n-hept-yloxy-2,5-dinitro-benzene.
2009 Dec 4
Reactions within p-difluorobenzene/methanol heterocluster ions: a detailed experimental and theoretical investigation.
2009 Mar 19
[Evaluation of two hydroxyl-terminated monocationic ionic liquid stationary phases with high thermal stability for capillary gas chromatography].
2010 Aug
N-(2,5-Dimeth-oxy-phen-yl)-N'-(4-hy-droxy-pheneth-yl)urea.
2010 Oct 2
2,3-Dibromo-1-[4-(2,3-dibromo-4,5-di-meth-oxy-benz-yl)-2,5-dimeth-oxy-benz-yl]-4,5-dimeth-oxy-benzene.
2010 Oct 31
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:01:34 GMT 2023
Edited
by admin
on Fri Dec 15 16:01:34 GMT 2023
Record UNII
24WC6T6X0G
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
1,4-DIMETHOXYBENZENE
Systematic Name English
BENZENE, P-DIMETHOXY-
Common Name English
FEMA NO. 2386
Code English
P-DIMETHOXYBENZENE [FHFI]
Common Name English
HYDROQUINONE DIMETHYL ETHER
HSDB  
Systematic Name English
BENZENE, 1,4-DIMETHOXY-
Systematic Name English
P-METHOXYANISOLE
Common Name English
HYDROQUINONE DIMETHYL ETHER [HSDB]
Common Name English
PARA-DIMETHYL HYDROQUINONE
Systematic Name English
PARA-DIMETHOXYBENZENE
Systematic Name English
P-DIMETHOXYBENZENE
FHFI  
Common Name English
NSC-7483
Code English
Classification Tree Code System Code
JECFA EVALUATION P-DIMETHOXYBENZENE
Created by admin on Fri Dec 15 16:01:34 GMT 2023 , Edited by admin on Fri Dec 15 16:01:34 GMT 2023
CFR 21 CFR 172.515
Created by admin on Fri Dec 15 16:01:34 GMT 2023 , Edited by admin on Fri Dec 15 16:01:34 GMT 2023
Code System Code Type Description
EVMPD
SUB129739
Created by admin on Fri Dec 15 16:01:34 GMT 2023 , Edited by admin on Fri Dec 15 16:01:34 GMT 2023
PRIMARY
ECHA (EC/EINECS)
205-771-9
Created by admin on Fri Dec 15 16:01:34 GMT 2023 , Edited by admin on Fri Dec 15 16:01:34 GMT 2023
PRIMARY
SMS_ID
100000155763
Created by admin on Fri Dec 15 16:01:34 GMT 2023 , Edited by admin on Fri Dec 15 16:01:34 GMT 2023
PRIMARY
FDA UNII
24WC6T6X0G
Created by admin on Fri Dec 15 16:01:34 GMT 2023 , Edited by admin on Fri Dec 15 16:01:34 GMT 2023
PRIMARY
JECFA MONOGRAPH
1259
Created by admin on Fri Dec 15 16:01:34 GMT 2023 , Edited by admin on Fri Dec 15 16:01:34 GMT 2023
PRIMARY
EPA CompTox
DTXSID0022014
Created by admin on Fri Dec 15 16:01:34 GMT 2023 , Edited by admin on Fri Dec 15 16:01:34 GMT 2023
PRIMARY
WIKIPEDIA
1,4-DIMETHOXYBENZENE
Created by admin on Fri Dec 15 16:01:34 GMT 2023 , Edited by admin on Fri Dec 15 16:01:34 GMT 2023
PRIMARY
CAS
150-78-7
Created by admin on Fri Dec 15 16:01:34 GMT 2023 , Edited by admin on Fri Dec 15 16:01:34 GMT 2023
PRIMARY
MESH
C031200
Created by admin on Fri Dec 15 16:01:34 GMT 2023 , Edited by admin on Fri Dec 15 16:01:34 GMT 2023
PRIMARY
HSDB
4259
Created by admin on Fri Dec 15 16:01:34 GMT 2023 , Edited by admin on Fri Dec 15 16:01:34 GMT 2023
PRIMARY
PUBCHEM
9016
Created by admin on Fri Dec 15 16:01:34 GMT 2023 , Edited by admin on Fri Dec 15 16:01:34 GMT 2023
PRIMARY
NSC
7483
Created by admin on Fri Dec 15 16:01:34 GMT 2023 , Edited by admin on Fri Dec 15 16:01:34 GMT 2023
PRIMARY