Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C8H9Br |
| Molecular Weight | 185.061 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
BrCCC1=CC=CC=C1
InChI
InChIKey=WMPPDTMATNBGJN-UHFFFAOYSA-N
InChI=1S/C8H9Br/c9-7-6-8-4-2-1-3-5-8/h1-5H,6-7H2
| Molecular Formula | C8H9Br |
| Molecular Weight | 185.061 |
| 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 |
|---|---|---|
| A novel histone deacetylase inhibitor exhibits antitumor activity via apoptosis induction, F-actin disruption and gene acetylation in lung cancer. | 2010-09-14 |
|
| Targeted LC-MS derivatization for aldehydes and carboxylic acids with a new derivatization agent 4-APEBA. | 2010-05 |
|
| Chlorogenate hydrolase-catalyzed synthesis of hydroxycinnamic acid ester derivatives by transesterification, substitution of bromine, and condensation reactions. | 2005-08 |
|
| The radical trap in atom transfer radical polymerization need not be thermodynamically stable. A study of the MoX(3)(PMe(3))(3) catalysts. | 2005-04-27 |
|
| Correlation of the rates of solvolysis of 2-phenyl-2-ketoethyl bromide and tosylate. | 2005-02-18 |
|
| Preparation and electrochemical behaviour of hydrophobic vitamin B(12) covalently immobilized onto platinum electrode. | 2004-01-07 |
|
| Antiangiogenic and antitumor agents. Design, synthesis, and evaluation of novel 2-amino-4-(3-bromoanilino)-6-benzylsubstituted pyrrolo[2,3-d]pyrimidines as inhibitors of receptor tyrosine kinases. | 2003-11-17 |
|
| Caffeic acid phenethyl ester (CAPE): synthesis and X-ray crystallographic analysis. | 2001-02 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:26:38 GMT 2025
by
admin
on
Mon Mar 31 21:26:38 GMT 2025
|
| Record UNII |
96O442668X
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Systematic Name | English | ||
|
Preferred Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Code | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
7666
Created by
admin on Mon Mar 31 21:26:38 GMT 2025 , Edited by admin on Mon Mar 31 21:26:38 GMT 2025
|
PRIMARY | |||
|
5352
Created by
admin on Mon Mar 31 21:26:38 GMT 2025 , Edited by admin on Mon Mar 31 21:26:38 GMT 2025
|
PRIMARY | |||
|
96O442668X
Created by
admin on Mon Mar 31 21:26:38 GMT 2025 , Edited by admin on Mon Mar 31 21:26:38 GMT 2025
|
PRIMARY | |||
|
33926
Created by
admin on Mon Mar 31 21:26:38 GMT 2025 , Edited by admin on Mon Mar 31 21:26:38 GMT 2025
|
PRIMARY | |||
|
2-Phenylethyl bromide
Created by
admin on Mon Mar 31 21:26:38 GMT 2025 , Edited by admin on Mon Mar 31 21:26:38 GMT 2025
|
PRIMARY | |||
|
103-63-9
Created by
admin on Mon Mar 31 21:26:38 GMT 2025 , Edited by admin on Mon Mar 31 21:26:38 GMT 2025
|
PRIMARY | |||
|
DTXSID1033876
Created by
admin on Mon Mar 31 21:26:38 GMT 2025 , Edited by admin on Mon Mar 31 21:26:38 GMT 2025
|
PRIMARY | |||
|
1269913
Created by
admin on Mon Mar 31 21:26:38 GMT 2025 , Edited by admin on Mon Mar 31 21:26:38 GMT 2025
|
PRIMARY | |||
|
203-130-8
Created by
admin on Mon Mar 31 21:26:38 GMT 2025 , Edited by admin on Mon Mar 31 21:26:38 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
PARENT -> IMPURITY |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
|
||
|
|
PARENT -> IMPURITY |
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
|
