Details
Stereochemistry | ACHIRAL |
Molecular Formula | C8H8O2 |
Molecular Weight | 136.1479 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=C(C=O)C=CC=C1
InChI
InChIKey=PKZJLOCLABXVMC-UHFFFAOYSA-N
InChI=1S/C8H8O2/c1-10-8-5-3-2-4-7(8)6-9/h2-6H,1H3
Molecular Formula | C8H8O2 |
Molecular Weight | 136.1479 |
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 |
---|---|---|
Solid-state photochromism and photoreactivity of o- and p-anisaldehydes. Remarkable stabilization of o-xylylenols. | 2001 May 17 |
|
Enantioselective synthesis of the AB-ring system of the antitumor antibiotic tetrazomine. | 2001 May 4 |
|
Mechanistic studies on the B(C(6)F(5))(3) catalyzed allylstannation of aromatic aldehydes with ortho donor substituents. | 2002 Feb 20 |
|
An experimental and computational evaluation of the energetics of the isomeric methoxyphenylcarbenes generated in carbon atom reactions. | 2002 Jan 16 |
|
Remarkably favorable hydration of carbonyl substituents in dicationic bis(arene) ruthenium complexes. | 2003 Feb 5 |
|
A novel potato defence-related alcohol:NADP+ oxidoreductase induced in response to Erwinia carotovora. | 2003 May |
|
Discovery of [4-Amino-2-(1-methanesulfonylpiperidin-4-ylamino)pyrimidin-5-yl](2,3-difluoro-6- methoxyphenyl)methanone (R547), a potent and selective cyclin-dependent kinase inhibitor with significant in vivo antitumor activity. | 2006 Nov 2 |
|
Aqueous Barbier allylation of aldehydes mediated by tin. | 2007 Aug 29 |
|
Oligonucleotides containing 6-aza-2'-deoxyuridine: synthesis, nucleobase protection, pH-dependent duplex stability, and metal-DNA formation. | 2007 Jun 8 |
|
Hantzsch synthesis of 2,6-dimethyl-3,5-dimethoxycarbonyl-4-(o-methoxyphenyl)-1,4-dihydropyridine; a novel cyclisation leading to an unusual formation of 1-amino-2-methoxy-carbonyl-3,5-bis(o-methoxyphenyl)-4-oxa-cyclohexan-1-ene. | 2007 Nov 26 |
|
N'-(2-Hydr-oxy-4-methoxy-benzyl-idene)-4-methoxy-benzohydrazide. | 2009 Aug 22 |
|
12-(2-Methoxyphenyl)-9,9-dimethyl-8,9-dihydro-12H-benzo[a]xanthen-11(10H)-one. | 2009 Dec 12 |
|
N'-(2-Methoxy-benzyl-idene)-2-nitro-benzo-hydrazide. | 2009 Feb 21 |
|
2-Methoxy-benzaldehyde 2,4-dinitro-phenyl-hydrazone. | 2009 Jan 8 |
|
New chiral thiophene-salen chromium complexes for the asymmetric Henry reaction. | 2009 Mar 6 |
|
4-Meth-oxy-N'-(2-methoxy-benzyl-idene)benzohydrazide. | 2009 May 23 |
|
1,1'-[4-(2-Methoxyphenyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-diyl]diethanone. | 2009 Oct 28 |
|
Diiodido[N'-(2-methoxy-benzyl-idene)-N,N-dimethyl-ethane-1,2-diamine]zinc(II). | 2009 Sep 19 |
|
4a-Hy-droxy-9-(2-meth-oxy-phen-yl)-4,4a,5,6,7,8,9,9a-octa-hydro-3H-xanthene-1,8(2H)-dione. | 2010 Dec 4 |
|
7-Chloro-4-[(E)-2-(2-methoxy-benzyl-idene)hydrazin-1-yl]quinoline monohydrate. | 2010 Feb 27 |
|
Antifungal activity of redox-active benzaldehydes that target cellular antioxidation. | 2011 May 31 |
|
Interesting anticandidal effects of anisic aldehydes on growth and proton-pumping-ATPase-targeted activity. | 2011 Oct |
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 18:03:13 UTC 2023
by
admin
on
Fri Dec 15 18:03:13 UTC 2023
|
Record UNII |
7CP821WF2W
|
Record Status |
Validated (UNII)
|
Record Version |
|
-
Download
Name | Type | Language | ||
---|---|---|---|---|
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Common Name | English |
Classification Tree | Code System | Code | ||
---|---|---|---|---|
|
CFR |
21 CFR 172.515
Created by
admin on Fri Dec 15 18:03:13 UTC 2023 , Edited by admin on Fri Dec 15 18:03:13 UTC 2023
|
||
|
JECFA EVALUATION |
O-ANISALDEHYDE
Created by
admin on Fri Dec 15 18:03:13 UTC 2023 , Edited by admin on Fri Dec 15 18:03:13 UTC 2023
|
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
58960
Created by
admin on Fri Dec 15 18:03:13 UTC 2023 , Edited by admin on Fri Dec 15 18:03:13 UTC 2023
|
PRIMARY | |||
|
DTXSID1051690
Created by
admin on Fri Dec 15 18:03:13 UTC 2023 , Edited by admin on Fri Dec 15 18:03:13 UTC 2023
|
PRIMARY | |||
|
8658
Created by
admin on Fri Dec 15 18:03:13 UTC 2023 , Edited by admin on Fri Dec 15 18:03:13 UTC 2023
|
PRIMARY | |||
|
7CP821WF2W
Created by
admin on Fri Dec 15 18:03:13 UTC 2023 , Edited by admin on Fri Dec 15 18:03:13 UTC 2023
|
PRIMARY | |||
|
1036948
Created by
admin on Fri Dec 15 18:03:13 UTC 2023 , Edited by admin on Fri Dec 15 18:03:13 UTC 2023
|
PRIMARY | |||
|
2-Methoxybenzaldehyde
Created by
admin on Fri Dec 15 18:03:13 UTC 2023 , Edited by admin on Fri Dec 15 18:03:13 UTC 2023
|
PRIMARY | |||
|
2039
Created by
admin on Fri Dec 15 18:03:13 UTC 2023 , Edited by admin on Fri Dec 15 18:03:13 UTC 2023
|
PRIMARY | |||
|
205-171-7
Created by
admin on Fri Dec 15 18:03:13 UTC 2023 , Edited by admin on Fri Dec 15 18:03:13 UTC 2023
|
PRIMARY | |||
|
135-02-4
Created by
admin on Fri Dec 15 18:03:13 UTC 2023 , Edited by admin on Fri Dec 15 18:03:13 UTC 2023
|
PRIMARY | |||
|
1992076
Created by
admin on Fri Dec 15 18:03:13 UTC 2023 , Edited by admin on Fri Dec 15 18:03:13 UTC 2023
|
PRIMARY | |||
|
7CP821WF2W
Created by
admin on Fri Dec 15 18:03:13 UTC 2023 , Edited by admin on Fri Dec 15 18:03:13 UTC 2023
|
PRIMARY |