Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C2H5BrO |
| Molecular Weight | 124.964 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OCCBr
InChI
InChIKey=LDLCZOVUSADOIV-UHFFFAOYSA-N
InChI=1S/C2H5BrO/c3-1-2-4/h4H,1-2H2
| Molecular Formula | C2H5BrO |
| Molecular Weight | 124.965 |
| 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 |
|---|---|---|
| The involvement of cytochrome P4502E1 in 2-bromoethanol-induced hepatocyte cytotoxicity. | 1996 Apr |
|
| Efficient synthesis of the cholinephosphate phospholipid headgroup. | 2001 Feb |
|
| Assessment of cancer risk from ethylene oxide residues in spices imported into New Zealand. | 2001 Nov |
|
| Determination of ethylene oxide by solid-phase microextraction device with on-fiber derivatization. | 2003 Mar 28 |
|
| Crystal structures and topochemical polymerizations of 7,7,8,8-tetrakis(alkoxycarbonyl)quinodimethanes. | 2004 Feb 25 |
|
| On the edge of the denaturation process: application of X-ray diffraction to barnase and lysozyme cross-linked crystals with denaturants in molar concentrations. | 2006 May |
|
| Rapid determination of ethylene oxide with fiber-packed sample preparation needle. | 2009 Apr 3 |
|
| 2-Hydroxy-ethyl 2-(2,4-dichloro-anilino)-4,4-dimethyl-6-oxocyclo-hex-1-ene-carbo-dithio-ate. | 2009 Feb 25 |
|
| Modeling the rovibrationally excited C2H4OH radicals from the photodissociation of 2-bromoethanol at 193 nm. | 2010 Apr 15 |
|
| A short stereoselective synthesis of racemic 2-epicalvine. | 2010 Aug |
|
| 1-Bromo-2-(10β-dihydro-artemisin-oxy)ethane. | 2010 Jul 31 |
|
| Stress sensing in polycaprolactone films via an embedded photochromic compound. | 2010 Jun |
|
| D-atom products in predissociation of CD2CD2OH from the 202-215 nm photodissociation of 2-bromoethanol. | 2010 May 6 |
|
| Glycoconjugates, products of uridine derivatives phosphitylation and oxidation as glycosyltransferases potential inhibitors. | 2010 Nov-Dec |
|
| Preservatives in cosmetics: reactivity of allergenic formaldehyde-releasers towards amino acids through breakdown products other than formaldehyde. | 2010 Oct |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 16:39:48 GMT 2023
by
admin
on
Fri Dec 15 16:39:48 GMT 2023
|
| Record UNII |
Z33995S34R
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Code | English | ||
|
Common Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
540-51-2
Created by
admin on Fri Dec 15 16:39:48 GMT 2023 , Edited by admin on Fri Dec 15 16:39:48 GMT 2023
|
PRIMARY | |||
|
C025475
Created by
admin on Fri Dec 15 16:39:49 GMT 2023 , Edited by admin on Fri Dec 15 16:39:49 GMT 2023
|
PRIMARY | |||
|
m5116
Created by
admin on Fri Dec 15 16:39:49 GMT 2023 , Edited by admin on Fri Dec 15 16:39:49 GMT 2023
|
PRIMARY | Merck Index | ||
|
2869
Created by
admin on Fri Dec 15 16:39:49 GMT 2023 , Edited by admin on Fri Dec 15 16:39:49 GMT 2023
|
PRIMARY | |||
|
10898
Created by
admin on Fri Dec 15 16:39:49 GMT 2023 , Edited by admin on Fri Dec 15 16:39:49 GMT 2023
|
PRIMARY | |||
|
Z33995S34R
Created by
admin on Fri Dec 15 16:39:49 GMT 2023 , Edited by admin on Fri Dec 15 16:39:49 GMT 2023
|
PRIMARY | |||
|
DTXSID8020200
Created by
admin on Fri Dec 15 16:39:48 GMT 2023 , Edited by admin on Fri Dec 15 16:39:48 GMT 2023
|
PRIMARY | |||
|
208-748-1
Created by
admin on Fri Dec 15 16:39:48 GMT 2023 , Edited by admin on Fri Dec 15 16:39:48 GMT 2023
|
PRIMARY |