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Details

Stereochemistry ACHIRAL
Molecular Formula C17H16Br2O3
Molecular Weight 428.115
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BROMOPROPYLATE

SMILES

CC(C)OC(=O)C(O)(C1=CC=C(Br)C=C1)C2=CC=C(Br)C=C2

InChI

InChIKey=FOANIXZHAMJWOI-UHFFFAOYSA-N
InChI=1S/C17H16Br2O3/c1-11(2)22-16(20)17(21,12-3-7-14(18)8-4-12)13-5-9-15(19)10-6-13/h3-11,21H,1-2H3

HIDE SMILES / InChI

Molecular Formula C17H16Br2O3
Molecular Weight 428.115
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Widely used pesticides with previously unknown endocrine activity revealed as in vitro antiandrogens.
2011-06
Comparative study of human and mouse pregnane X receptor agonistic activity in 200 pesticides using in vitro reporter gene assays.
2011-02-27
Preparation of activated carbons from agricultural residues for pesticide adsorption.
2010-09
Evaluation of immunoassays as an alternative for the rapid determination of pesticides in wine and grape samples.
2010-03-26
Development of an enzyme-linked immunosorbent assay for determination of the miticide bromopropylate.
2009-01-28
Estimating half-lives of pesticides in/on vegetation for use in multimedia fate and exposure models.
2008-02
Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods.
2006-11
Screening for estrogen and androgen receptor activities in 200 pesticides by in vitro reporter gene assays using Chinese hamster ovary cells.
2004-04
Determination of impurities in pesticides and their degradation products formed during the wine-making process by solid-phase extraction and gas chromatography with detection by electron ionization mass spectrometry. II. Bromopropylate, trichlorphon, parathion-methyl and tebuconazole.
2004
Rapid multi-residue method for the determination of azinphos methyl, bromopropylate, chlorpyrifos, dimethoate, parathion methyl and phosalone in apricots and peaches by using negative chemical ionization ion trap technology.
2003-05-09
Promotion of altered hepatic foci development in rat liver, cytochrome P450 enzyme induction and inhibition of cell-cell communication by DDT and some structurally related organohalogen pesticides.
1990-08
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:53:06 GMT 2025
Edited
by admin
on Mon Mar 31 18:53:06 GMT 2025
Record UNII
3U468ZM257
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-195087
Preferred Name English
BROMOPROPYLATE
HSDB   ISO   MI  
Common Name English
1-METHYLETHYL 4-BROMO-.ALPHA.-(4-BROMOPHENYL)-.ALPHA.-HYDROXYBENZENEACETATE
Systematic Name English
ISOPROPYL 4,4'-DIBROMOBENZILATE
Systematic Name English
BROMOPROPYLATE [ISO]
Common Name English
BROMOPROPYLATE [MI]
Common Name English
BROMOPROPYLATE [HSDB]
Common Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 28802
Created by admin on Mon Mar 31 18:53:06 GMT 2025 , Edited by admin on Mon Mar 31 18:53:06 GMT 2025
WHO-VATC QP53AX14
Created by admin on Mon Mar 31 18:53:06 GMT 2025 , Edited by admin on Mon Mar 31 18:53:06 GMT 2025
Code System Code Type Description
EPA CompTox
DTXSID1034397
Created by admin on Mon Mar 31 18:53:06 GMT 2025 , Edited by admin on Mon Mar 31 18:53:06 GMT 2025
PRIMARY
WIKIPEDIA
BROMOPROPYLATE
Created by admin on Mon Mar 31 18:53:06 GMT 2025 , Edited by admin on Mon Mar 31 18:53:06 GMT 2025
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HSDB
1731
Created by admin on Mon Mar 31 18:53:06 GMT 2025 , Edited by admin on Mon Mar 31 18:53:06 GMT 2025
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SMS_ID
300000031279
Created by admin on Mon Mar 31 18:53:06 GMT 2025 , Edited by admin on Mon Mar 31 18:53:06 GMT 2025
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MESH
C038267
Created by admin on Mon Mar 31 18:53:06 GMT 2025 , Edited by admin on Mon Mar 31 18:53:06 GMT 2025
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FDA UNII
3U468ZM257
Created by admin on Mon Mar 31 18:53:06 GMT 2025 , Edited by admin on Mon Mar 31 18:53:06 GMT 2025
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ALANWOOD
bromopropylate
Created by admin on Mon Mar 31 18:53:06 GMT 2025 , Edited by admin on Mon Mar 31 18:53:06 GMT 2025
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PUBCHEM
28936
Created by admin on Mon Mar 31 18:53:06 GMT 2025 , Edited by admin on Mon Mar 31 18:53:06 GMT 2025
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CAS
18181-80-1
Created by admin on Mon Mar 31 18:53:06 GMT 2025 , Edited by admin on Mon Mar 31 18:53:06 GMT 2025
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MERCK INDEX
m2715
Created by admin on Mon Mar 31 18:53:06 GMT 2025 , Edited by admin on Mon Mar 31 18:53:06 GMT 2025
PRIMARY Merck Index
NSC
195087
Created by admin on Mon Mar 31 18:53:06 GMT 2025 , Edited by admin on Mon Mar 31 18:53:06 GMT 2025
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ECHA (EC/EINECS)
242-070-7
Created by admin on Mon Mar 31 18:53:06 GMT 2025 , Edited by admin on Mon Mar 31 18:53:06 GMT 2025
PRIMARY