Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C3H4Br2 |
| Molecular Weight | 199.872 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
BrCC(Br)=C
InChI
InChIKey=YMFWYDYJHRGGPF-UHFFFAOYSA-N
InChI=1S/C3H4Br2/c1-3(5)2-4/h1-2H2
| Molecular Formula | C3H4Br2 |
| Molecular Weight | 199.872 |
| 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 |
|---|---|---|
| Formal synthesis of (+/-)-platensimycin. | 2007-04-26 |
|
| Identification of glutathione conjugates of 2, 3-dibromopropene in male ICR mice. | 2006-02 |
|
| Novel carbonyl bromoallylation/Heck reaction sequence. Stereocontrolled access to bicyclic beta-lactams. | 2005-04-01 |
|
| Straightforward asymmetric entry to highly functionalized 3-substituted 3-hydroxy-beta-lactams via Baylis-Hillman or bromoallylation reactions. | 2004-02-06 |
|
| Haloalkane dehalogenase LinB from Sphingomonas paucimobilis UT26: X-ray crystallographic studies of dehalogenation of brominated substrates. | 2003-09-02 |
|
| Controlling chemoselectivity in vinyl and allylic C-X bond activation with palladium catalysis: a pK(a)-based electronic switch. | 2002-02-20 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:07:28 GMT 2025
by
admin
on
Mon Mar 31 21:07:28 GMT 2025
|
| Record UNII |
8DNE7K7Z6P
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
8DNE7K7Z6P
Created by
admin on Mon Mar 31 21:07:28 GMT 2025 , Edited by admin on Mon Mar 31 21:07:28 GMT 2025
|
PRIMARY | |||
|
513-31-5
Created by
admin on Mon Mar 31 21:07:28 GMT 2025 , Edited by admin on Mon Mar 31 21:07:28 GMT 2025
|
PRIMARY | |||
|
DTXSID9060152
Created by
admin on Mon Mar 31 21:07:28 GMT 2025 , Edited by admin on Mon Mar 31 21:07:28 GMT 2025
|
PRIMARY | |||
|
208-155-8
Created by
admin on Mon Mar 31 21:07:28 GMT 2025 , Edited by admin on Mon Mar 31 21:07:28 GMT 2025
|
PRIMARY | |||
|
10552
Created by
admin on Mon Mar 31 21:07:28 GMT 2025 , Edited by admin on Mon Mar 31 21:07:28 GMT 2025
|
PRIMARY | |||
|
m4300
Created by
admin on Mon Mar 31 21:07:28 GMT 2025 , Edited by admin on Mon Mar 31 21:07:28 GMT 2025
|
PRIMARY | Merck Index | ||
|
6200
Created by
admin on Mon Mar 31 21:07:28 GMT 2025 , Edited by admin on Mon Mar 31 21:07:28 GMT 2025
|
PRIMARY |