Details
Stereochemistry | RACEMIC |
Molecular Formula | C3H6O2 |
Molecular Weight | 74.0785 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
OCC1CO1
InChI
InChIKey=CTKINSOISVBQLD-UHFFFAOYSA-N
InChI=1S/C3H6O2/c4-1-3-2-5-3/h3-4H,1-2H2
Molecular Formula | C3H6O2 |
Molecular Weight | 74.0785 |
Charge | 0 |
Count |
|
Stereochemistry | RACEMIC |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Optical Activity | ( + / - ) |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Examination of low-incidence brain tumor responses in F344 rats following chemical exposures in National Toxicology Program carcinogenicity studies. | 1999 Sep-Oct |
|
A convenient chiron for substituted cyclohexanones. | 2001 Aug 24 |
|
Expedient access to the okadaic acid architecture: a novel synthesis of the C1-C27 domain. | 2001 Feb 9 |
|
Synthesis of the C1-C12 fragment of fostriecin. | 2001 Jul 12 |
|
Point mutations of K-ras and H-ras genes in forestomach neoplasms from control B6C3F1 mice and following exposure to 1,3-butadiene, isoprene or chloroprene for up to 2-years. | 2001 Jun 1 |
|
Interpreting the signal from a localized fluorescence sensor: a study by angle-resolved XPS and dynamic SIMS. | 2003 Jun 15 |
|
Basis set and density functional dependence of vibrational Raman optical activity calculations. | 2005 Aug 25 |
|
Hydrophilic core-shell microspheres: a suitable support for controlled attachment of proteins and biomedical diagnostics. | 2005 Dec 15 |
|
Poly(amidoamine) dendrimer-based multifunctional engineered nanodevice for cancer therapy. | 2005 Sep 22 |
|
Chemical variation of natural product-like scaffolds: design and synthesis of spiroketal derivatives. | 2006 May 21 |
|
Biocatalytic approaches to optically active beta-blockers. | 2007 |
|
Preparation of liquid-core nanocapsules from poly[(ethylene oxide)-co-glycidol] with multiple hydrophobic linoleates at an oil-water interface and its encapsulation of pyrene. | 2007 Jun |
|
Oxiranylmethyloxy or thiiranylmethyloxy-azaxanthones and -acridone analogues as potential topoisomerase I inhibitors. | 2009 Dec 1 |
|
Enzymatic one-pot route to telechelic polypentadecalactone epoxide: synthesis, UV curing, and characterization. | 2009 Nov 9 |
|
A new analytical method for the quantification of glycidol fatty acid esters in edible oils. | 2010 |
|
Substrate-controlled asymmetric total synthesis and structure revision of (+)-itomanallene A. | 2010 |
|
Significant changes in the transesterification activity of free and mesoporous-immobilized Rhizopus oryzae lipase in ionic liquids. | 2010 Feb 1 |
|
A spectroscopic and computational investigation of the conformational structural changes induced by hydrogen bonding networks in the glycidol-water complex. | 2010 Jan 14 |
|
Hyperbranched polyglycerols: from the controlled synthesis of biocompatible polyether polyols to multipurpose applications. | 2010 Jan 19 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 17:35:22 GMT 2025
by
admin
on
Mon Mar 31 17:35:22 GMT 2025
|
Record UNII |
S54CF1DV9A
|
Record Status |
Validated (UNII)
|
Record Version |
|
-
Download
Name | Type | Language | ||
---|---|---|---|---|
|
Preferred Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English |
Classification Tree | Code System | Code | ||
---|---|---|---|---|
|
NCI_THESAURUS |
C45408
Created by
admin on Mon Mar 31 17:35:22 GMT 2025 , Edited by admin on Mon Mar 31 17:35:22 GMT 2025
|
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
556-52-5
Created by
admin on Mon Mar 31 17:35:22 GMT 2025 , Edited by admin on Mon Mar 31 17:35:22 GMT 2025
|
PRIMARY | |||
|
C44387
Created by
admin on Mon Mar 31 17:35:22 GMT 2025 , Edited by admin on Mon Mar 31 17:35:22 GMT 2025
|
PRIMARY | |||
|
GLYCIDOL
Created by
admin on Mon Mar 31 17:35:22 GMT 2025 , Edited by admin on Mon Mar 31 17:35:22 GMT 2025
|
PRIMARY | |||
|
1819
Created by
admin on Mon Mar 31 17:35:22 GMT 2025 , Edited by admin on Mon Mar 31 17:35:22 GMT 2025
|
PRIMARY | |||
|
m5795
Created by
admin on Mon Mar 31 17:35:22 GMT 2025 , Edited by admin on Mon Mar 31 17:35:22 GMT 2025
|
PRIMARY | Merck Index | ||
|
300000053404
Created by
admin on Mon Mar 31 17:35:22 GMT 2025 , Edited by admin on Mon Mar 31 17:35:22 GMT 2025
|
PRIMARY | |||
|
DTXSID4020666
Created by
admin on Mon Mar 31 17:35:22 GMT 2025 , Edited by admin on Mon Mar 31 17:35:22 GMT 2025
|
PRIMARY | |||
|
30966
Created by
admin on Mon Mar 31 17:35:22 GMT 2025 , Edited by admin on Mon Mar 31 17:35:22 GMT 2025
|
PRIMARY | |||
|
S54CF1DV9A
Created by
admin on Mon Mar 31 17:35:22 GMT 2025 , Edited by admin on Mon Mar 31 17:35:22 GMT 2025
|
PRIMARY | |||
|
46096
Created by
admin on Mon Mar 31 17:35:22 GMT 2025 , Edited by admin on Mon Mar 31 17:35:22 GMT 2025
|
PRIMARY | |||
|
209-128-3
Created by
admin on Mon Mar 31 17:35:22 GMT 2025 , Edited by admin on Mon Mar 31 17:35:22 GMT 2025
|
PRIMARY | |||
|
11164
Created by
admin on Mon Mar 31 17:35:22 GMT 2025 , Edited by admin on Mon Mar 31 17:35:22 GMT 2025
|
PRIMARY | |||
|
C004312
Created by
admin on Mon Mar 31 17:35:22 GMT 2025 , Edited by admin on Mon Mar 31 17:35:22 GMT 2025
|
PRIMARY |
Related Record | Type | Details | ||
---|---|---|---|---|
|
PARENT -> IMPURITY |
fatty acid esters of GLYCIDOL also present
|
||
|
PARENT -> IMPURITY |
CHROMATOGRAPHIC PURITY (GC)
EP
|