4-CHLOROANISOLE

Details

Stereochemistry	ACHIRAL
Molecular Formula	C7H7ClO
Molecular Weight	142.583
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

COC1=CC=C(Cl)C=C1

InChI

InChIKey=YRGAYAGBVIXNAQ-UHFFFAOYSA-N

InChI=1S/C7H7ClO/c1-9-7-4-2-6(8)3-5-7/h2-5H,1H3

HIDE SMILES / InChI

Molecular Formula	C7H7ClO
Molecular Weight	142.583
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Approval Year

PubMed

Title	Date	PubMed
Biodegradation of the major color containing compounds in distillery wastewater by an aerobic bacterial culture and characterization of their metabolites.	2010-09	20146090
Cavity-shaped ligands: calix[4]arene-based monophosphanes for fast Suzuki-Miyaura cross-coupling.	2010-08-09	20583042
Surface photochemistry of pesticides containing 4-chlorophenoxyl chromophore.	2010-07-15	20334970
Photochemistry of 4-chlorophenol and 4-chloroanisole adsorbed on MFI zeolites: supramolecular control of chemoselectivity and reactive intermediate dynamics.	2010-07-02	20527903
Glucose as a clean and renewable reductant in the Pd-nanoparticle-catalyzed reductive homocoupling of bromo- and chloroarenes in water.	2010-06-04	20462265
Dechlorination/detoxification of aromatic chlorides using fly ash under mild conditions.	2009-12	19740644
Synthesis of a carbene transfer organometallic polymer and application to forming a recyclable heterogeneous catalyst for the Suzuki reactions of aryl chlorides.	2009-10-21	19789786
N-donor functionalized N-heterocyclic carbene nickel(II) complexes in the Kumada coupling.	2009-09-21	20449135
Palladium-catalyzed aminations of aryl halides with phosphine-functionalized imidazolium ligands.	2008-02-21	18259628
Revealing phenylium, phenonium, vinylenephenonium, and benzenium ions in solution.	2008	18000926
Calcium-promoted catalytic degradation of PCDDs, PCDFs, and coplanar PCBs under a mild wet process.	2006-03-15	16570607
Synthesis, anti-HIV activity, and metabolic stability of new alkenyldiarylmethane HIV-1 non-nucleoside reverse transcriptase inhibitors.	2005-09-22	16162014
Production of fungal biomass immobilized loofa sponge (FBILS)-discs for the removal of heavy metal ions and chlorinated compounds from aqueous solution.	2005-09	16215832
Synthesis, characterization, and PGSE (1H and 19F) NMR diffusion studies on cationic (eta6- arene)Mn(CO)3+ complexes: boron counterion, ion pairing, and solvent dependences.	2005-08-08	16060650
(5-Arylfuran-2-ylcarbonyl)guanidines as cardioprotectives through the inhibition of Na+/H+ exchanger isoform-1.	2005-04-21	15828827
Aryl cations from aromatic halides. Photogeneration and reactivity of 4-hydroxy(methoxy)phenyl cation.	2004-05-14	15132557
Layered double hydroxide supported nanopalladium catalyst for Heck-, Suzuki-, Sonogashira-, and Stille-type coupling reactions of chloroarenes.	2002-11-27	12440911

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 19:13:29 GMT 2025` Edited by `admin` on `Mon Mar 31 19:13:29 GMT 2025`
Record UNII	0F18BLY08Q
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

NSC-4129

Preferred Name

English

4-CHLOROANISOLE

Systematic Name

English

1-CHLORO-4-METHOXYBENZENE

Systematic Name

English

4-CHLOROPHENOL METHYL ETHER

Systematic Name

English

4-METHOXYPHENYL CHLORIDE

Systematic Name

English

1-METHOXY-4-CHLOROBENZENE

Systematic Name

English

BENZENE, 1-CHLORO-4-METHOXY-

Systematic Name

English

4-METHOXYCHLOROBENZENE

Systematic Name

English

P-CHLOROMETHOXYBENZENE

Common Name

English

ANISOLE, P-CHLORO-

Common Name

English

P-METHOXYPHENYL CHLORIDE

Common Name

English

P-CHLOROANISOLE

Common Name

English

P-METHOXYCHLOROBENZENE

Common Name

English

4-CHLOROPHENYL METHYL ETHER

Systematic Name

English

P-CHLOROPHENYL METHYL ETHER

Common Name

English

Code System Code Type Description

FDA UNII

0F18BLY08Q