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Details

Stereochemistry ACHIRAL
Molecular Formula C5H8O
Molecular Weight 84.1164
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 3,4-DIHYDRO-2H-PYRAN

SMILES

C1COC=CC1

InChI

InChIKey=BUDQDWGNQVEFAC-UHFFFAOYSA-N
InChI=1S/C5H8O/c1-2-4-6-5-3-1/h2,4H,1,3,5H2

HIDE SMILES / InChI

Molecular Formula C5H8O
Molecular Weight 84.1164
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Total synthesis of microtubule-stabilizing agent (-)-laulimalide.
2001 Dec 28
Synthesis of plagiochiline N from santonin.
2001 Nov 16
Substituted alkenediols by alkylative double ring opening of dihydrofuran and dihydropyran epoxides.
2001 Oct 18
Stereoselective reactions of (20R)-3,20-dihydroxy-(3',4'-dihydro-2'H-pyranyl)-5-pregnene derivatives form 27-nor-3,20,23,26-tetrahydroxy-cholesten-22-ones and related bromo ketones.
2004 Jan
Biological activities of marine sesquiterpenoid quinones: structure-activity relationships in cytotoxic and hemolytic assays.
2004 Oct
Synthesis of 4-deoxy-L-(and D-)hexoses from chiral noncarbohydrate building blocks.
2004 Oct 15
Enantioselective total synthesis of (-)-candelalide A, a novel blocker of the voltage-gated potassium channel Kv1.3 for an immunosuppressive agent.
2005 Aug 18
Spiroacetal biosynthesis: (+/-)-1,7-dioxaspiro[5.5]undecane in Bactrocera cacuminata and Bactrocera oleae (Olive Fruit Fly).
2005 Mar 17
Imino Diels-Alder adducts. II. Two pyrano[3,2-c]quinolines.
2005 May
Synthesis of the C(43)-C(67) fragment of amphidinol 3.
2005 Nov 24
Stereoselective synthesis of spirocyclic ketones by Nazarov reaction.
2005 Sep 29
cis-3-Methyl-1-phenyl-8a,9,10,11,12,12a,12b-hexa-hydro-1H,3bH-pyrazolo[3,4:2',3']pyrano[4',5',6'-kl]xanthene.
2007 Dec 12
Nickel-catalyzed cycloadditions of unsaturated hydrocarbons, aldehydes, and ketones.
2008 Apr 4
Vinylic C--H borylation of cyclic vinyl ethers with bis(pinacolato)diboron catalyzed by an Iridium(I)-dtbpy complex.
2008 Dec 1
Potassium trifluoro-[(Z)-3-(oxan-2-yl-oxy)prop-1-en-1-yl]borate monohydrate.
2008 Dec 24
Hydrolytic reactivity trends among potential prodrugs of the O2-glycosylated diazeniumdiolate family. Targeting nitric oxide to macrophages for antileishmanial activity.
2008 Jul 10
Total synthesis of bryostatin 16 using atom-economical and chemoselective approaches.
2008 Nov 27
Stereocontrolled formal synthesis of (+/-)-platensimycin.
2008 Sep 18
Function-oriented synthesis: biological evaluation of laulimalide analogues derived from a last step cross metathesis diversification strategy.
2008 Sep-Oct
1-Ethyl-2-tosyl-4,4,6-trimethyl-2,3,3a,4-tetra-hydro-1H-pyrrolo[3,4-c]pyrano[6,5-b]quinoline-11(6H)-one monohydrate.
2009 Aug 8
cis-1-Ethyl-4,4,6,8-tetra-methyl-2-tosyl-2,3,3a,4,6,7,8,9-octa-hydro-1H-pyrrolo[3',4':3,4]pyrano[6,5-d]pyrimidine-7,9-dione.
2009 Jul 15
Synthesis, characterization and biological activity of ring-substituted 6-benzylamino-9-tetrahydropyran-2-yl and 9-tetrahydrofuran-2-ylpurine derivatives.
2009 Mar 1
Synthesis and structural characterization of two diasteroisomers of vinylcatechin dimers.
2009 Nov 11
1-Benzyl-6,8-dimethyl-4-phenyl-2-tosyl-1,2,3,3a,4,6,7,8,9,9b-deca-hydro-pyrrolo[3,4-c]pyrano[6,5-d]pyrimidine-7,9-dione.
2009 Oct 28
4,4-Dimethyl-2-tosyl-1,2,3,3a,4,11b-hexa-hydro-11H-pyrrolo[3,4-c]pyrano[5,6-c]chromen-11-one 0.125-hydrate.
2009 Oct 31
8-[(3,3-Dimethyl-oxiran-2-yl)methoxy-meth-yl]-11-hydr-oxy-2-isopropenyl-5-methyl-12-oxo-1,2,3,12-tetra-hydro-pyrano[3,2-a]xanthen-1-yl acetate.
2009 Sep 26
Racemic tricarbonyl[(4a,5,6,7,8,8a-η)-2-phenyl-3,4-dihydro-2H-1-benzopyran]chromium(0).
2010 Aug 11
Total synthesis of (+)-ambruticin S: probing the pharmacophoric subunit.
2010 Aug 20
Kinetic analysis of genipin degradation in aqueous solution.
2010 Dec
Racemic tricarbon-yl(η-7-meth-oxy-flavan)chromium(0).
2010 Jul 10
Total synthesis of jerangolid A.
2010 Jul 16
Methyl 4-(4-chloro-phen-yl)-3,3a,4,4a,5,12c-hexa-hydro-2-thia-naphtho-[1',2':3,2]furo[5,4-b]pyrrolizine-4a-carboxyl-ate.
2010 Jul 24
Methyl 4-phenyl-1,2,3,3a,4,4a,5,12c-octa-hydronaphtho[1',2':3,2]furo[5,4-b]pyrrolizine-4a-carboxyl-ate.
2010 May 15
Bioengineering functional copolymers. XIV. Synthesis and interaction of poly(N-isopropylacrylamide-co-3,4-dihydro-2H-pyran-alt-maleic anhydride)s with SCLC cancer cells.
2010 Nov 15
Coupling the Petasis condensation to an iron(III) chloride-promoted cascade provides a short synthesis of Relenza congeners.
2010 Nov 19
Cytotoxic terpene quinones from marine sponges.
2010 Nov 24
3-Ethyl 2-methyl 8-bromo-2-phenyl-1,2,3,3a,4,9b-hexa-hydro-chromeno[4,3-b]pyrrole-2,3-dicarboxyl-ate.
2010 Nov 6
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 19:12:06 GMT 2023
Edited
by admin
on Fri Dec 15 19:12:06 GMT 2023
Record UNII
T6V9N71IHX
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
3,4-DIHYDRO-2H-PYRAN
Systematic Name English
2,3-DIHYDRO-4H-PYRAN
Systematic Name English
2-PYRAN, 3,4-DIHYDRO-
Systematic Name English
1,2-PYRAN, 3,4-DIHYDRO-
Systematic Name English
DIHYDROPYRAN
MI  
Systematic Name English
NSC-73472
Code English
DIHYDRO-2H-PYRAN, 3,4-
Systematic Name English
3,4-DIHYDROPYRAN
Systematic Name English
2,3-DIHYDRO-.GAMMA.-PYRAN
Common Name English
DIHYDRO-2H-PYRAN
Systematic Name English
NSC-57860
Code English
PYRAN, DIHYDRO-
Systematic Name English
.DELTA.2-DIHYDROPYRAN
Common Name English
5,6-DIHYDRO-4H-PYRAN
Systematic Name English
2H-3,4-DIHYDROPYRAN
Common Name English
2H-PYRAN, 3,4-DIHYDRO-
Systematic Name English
DIHYDROPYRAN [MI]
Common Name English
Code System Code Type Description
PUBCHEM
8080
Created by admin on Fri Dec 15 19:12:06 GMT 2023 , Edited by admin on Fri Dec 15 19:12:06 GMT 2023
PRIMARY
FDA UNII
T6V9N71IHX
Created by admin on Fri Dec 15 19:12:06 GMT 2023 , Edited by admin on Fri Dec 15 19:12:06 GMT 2023
PRIMARY
CAS
110-87-2
Created by admin on Fri Dec 15 19:12:06 GMT 2023 , Edited by admin on Fri Dec 15 19:12:06 GMT 2023
PRIMARY
ECHA (EC/EINECS)
203-810-4
Created by admin on Fri Dec 15 19:12:06 GMT 2023 , Edited by admin on Fri Dec 15 19:12:06 GMT 2023
PRIMARY
EPA CompTox
DTXSID6041426
Created by admin on Fri Dec 15 19:12:06 GMT 2023 , Edited by admin on Fri Dec 15 19:12:06 GMT 2023
PRIMARY
MERCK INDEX
m4465
Created by admin on Fri Dec 15 19:12:06 GMT 2023 , Edited by admin on Fri Dec 15 19:12:06 GMT 2023
PRIMARY Merck Index
NSC
73472
Created by admin on Fri Dec 15 19:12:06 GMT 2023 , Edited by admin on Fri Dec 15 19:12:06 GMT 2023
PRIMARY
NSC
57860
Created by admin on Fri Dec 15 19:12:06 GMT 2023 , Edited by admin on Fri Dec 15 19:12:06 GMT 2023
PRIMARY
WIKIPEDIA
3,4-Dihydropyran
Created by admin on Fri Dec 15 19:12:06 GMT 2023 , Edited by admin on Fri Dec 15 19:12:06 GMT 2023
PRIMARY