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

Details

Stereochemistry ACHIRAL
Molecular Formula C11H12O
Molecular Weight 160.2124
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2,2-DIMETHYL-2H-1-BENZOPYRAN

SMILES

CC1(C)OC2=C(C=CC=C2)C=C1

InChI

InChIKey=SAXKWTPDZMBKSQ-UHFFFAOYSA-N
InChI=1S/C11H12O/c1-11(2)8-7-9-5-3-4-6-10(9)12-11/h3-8H,1-2H3

HIDE SMILES / InChI

Molecular Formula C11H12O
Molecular Weight 160.2124
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Identification of a novel small-molecule inhibitor of the hypoxia-inducible factor 1 pathway.
2005-01-15
A convenient and biogenetic type synthesis of few naturally occurring chromeno dihydrochalcones and their in vitro antileishmanial activity.
2004-08-02
Metalloporphyrin-mediated asymmetric nitrogen-atom transfer to hydrocarbons: aziridination of alkenes and amidation of saturated C-H bonds catalyzed by chiral ruthenium and manganese porphyrins.
2002-04-02
Dendritic ruthenium porphyrins: a new class of highly selective catalysts for alkene epoxidation and cyclopropanation.
2002-04-02
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 18:57:09 GMT 2025
Edited
by admin
on Mon Mar 31 18:57:09 GMT 2025
Record UNII
M07GJA13Z5
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FC 1
Preferred Name English
2,2-DIMETHYL-2H-1-BENZOPYRAN
Systematic Name English
2H-1-BENZOPYRAN, 2,2-DIMETHYL-
Systematic Name English
2,2-DIMETHYL-2H-CHROMENE
Systematic Name English
2,2-DIMETHYLBENZOPYRAN
Systematic Name English
1,2-BENZOPYRAN, 2,2-DIMETHYL-
Common Name English
2,2-DIMETHYL-3-CHROMENE
Common Name English
2,2-DIMETHYLCHROMENE
Systematic Name English
Code System Code Type Description
PUBCHEM
75642
Created by admin on Mon Mar 31 18:57:09 GMT 2025 , Edited by admin on Mon Mar 31 18:57:09 GMT 2025
PRIMARY
CAS
2513-25-9
Created by admin on Mon Mar 31 18:57:09 GMT 2025 , Edited by admin on Mon Mar 31 18:57:09 GMT 2025
PRIMARY
FDA UNII
M07GJA13Z5
Created by admin on Mon Mar 31 18:57:09 GMT 2025 , Edited by admin on Mon Mar 31 18:57:09 GMT 2025
PRIMARY
EPA CompTox
DTXSID70179813
Created by admin on Mon Mar 31 18:57:09 GMT 2025 , Edited by admin on Mon Mar 31 18:57:09 GMT 2025
PRIMARY