Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C8H8O3 |
| Molecular Weight | 152.1473 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OCC1=CC=CC=C1C(O)=O
InChI
InChIKey=MGMNPSAERQZUIM-UHFFFAOYSA-N
InChI=1S/C8H8O3/c9-5-6-3-1-2-4-7(6)8(10)11/h1-4,9H,5H2,(H,10,11)
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| 2-(Hydroxycarbonyl)benzyl glycosides: a novel type of glycosyl donors for highly efficient beta-mannopyranosylation and oligosaccharide synthesis by latent-active glycosylation. | 2001 Sep 5 |
|
| Synthesis of 2,4-diamino-6-[2'-O-(omega-carboxyalkyl)oxydibenz[b,f]azepin-5-yl]methylpteridines as potent and selective inhibitors of Pneumocystis carinii, Toxoplasma gondii, and Mycobacterium avium dihydrofolate reductase. | 2004 May 6 |
|
| Breakdown products on metabolic pathway of degradation of benz[a]anthracene by a ligninolytic fungus. | 2006 Jul |
|
| In vitro models in biocompatibility assessment for biomedical-grade chitosan derivatives in wound management. | 2009 Mar |
| Name | Type | Language | ||
|---|---|---|---|---|
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
DTXSID30210099
Created by
admin on Fri Dec 15 19:34:03 GMT 2023 , Edited by admin on Fri Dec 15 19:34:03 GMT 2023
|
PRIMARY | |||
|
KJ3Z1IJ8O3
Created by
admin on Fri Dec 15 19:34:03 GMT 2023 , Edited by admin on Fri Dec 15 19:34:03 GMT 2023
|
PRIMARY | |||
|
30638
Created by
admin on Fri Dec 15 19:34:03 GMT 2023 , Edited by admin on Fri Dec 15 19:34:03 GMT 2023
|
PRIMARY | |||
|
11920
Created by
admin on Fri Dec 15 19:34:03 GMT 2023 , Edited by admin on Fri Dec 15 19:34:03 GMT 2023
|
PRIMARY | |||
|
210-298-6
Created by
admin on Fri Dec 15 19:34:03 GMT 2023 , Edited by admin on Fri Dec 15 19:34:03 GMT 2023
|
PRIMARY | |||
|
612-20-4
Created by
admin on Fri Dec 15 19:34:03 GMT 2023 , Edited by admin on Fri Dec 15 19:34:03 GMT 2023
|
PRIMARY |
SUBSTANCE RECORD
