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 |
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Caffeic acid phenethyl ester (CAPE): synthesis and X-ray crystallographic analysis. | 2001 Feb |
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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 Nov 17 |
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Preparation and electrochemical behaviour of hydrophobic vitamin B(12) covalently immobilized onto platinum electrode. | 2004 Jan 7 |
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The radical trap in atom transfer radical polymerization need not be thermodynamically stable. A study of the MoX(3)(PMe(3))(3) catalysts. | 2005 Apr 27 |
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Chlorogenate hydrolase-catalyzed synthesis of hydroxycinnamic acid ester derivatives by transesterification, substitution of bromine, and condensation reactions. | 2005 Aug |
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Correlation of the rates of solvolysis of 2-phenyl-2-ketoethyl bromide and tosylate. | 2005 Feb 18 |
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Targeted LC-MS derivatization for aldehydes and carboxylic acids with a new derivatization agent 4-APEBA. | 2010 May |
|
A novel histone deacetylase inhibitor exhibits antitumor activity via apoptosis induction, F-actin disruption and gene acetylation in lung cancer. | 2010 Sep 14 |
Patents
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 05:09:55 GMT 2023
by
admin
on
Sat Dec 16 05:09:55 GMT 2023
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Record UNII |
96O442668X
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Record Status |
Validated (UNII)
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7666
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5352
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96O442668X
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33926
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2-Phenylethyl bromide
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103-63-9
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DTXSID1033876
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1269913
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203-130-8
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