추천 제품
Quality Level
분석
98%
양식
solid
bp
236 °C (lit.)
mp
28-32 °C (lit.)
작용기
bromo
SMILES string
Oc1cccc(Br)c1
InChI
1S/C6H5BrO/c7-5-2-1-3-6(8)4-5/h1-4,8H
InChI key
MNOJRWOWILAHAV-UHFFFAOYSA-N
유전자 정보
human ... ALOX12(239) , ALOX15(246)
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일반 설명
3-Bromophenol is used for suzuki-miyaura coupling reaction and in the synthesis of pentacyclic building block benzodibenzofuranquinone.
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
No data available
Flash Point (°C)
No data available
개인 보호 장비
dust mask type N95 (US), Eyeshields, Gloves
이미 열람한 고객
D Mahadevan et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 78(2), 575-581 (2010-12-28)
The FT-IR and FT-Raman spectra of 3-Bromo phenol (3-BP) molecule have been recorded using Bruker IFS 66V spectrometer in the range of 4000-100 cm(-1). The molecular geometry and vibrational frequencies in the ground state are calculated by using the ab
S Chakrabarti et al.
Environmental research, 39(1), 50-59 (1986-02-01)
When male Sprague-Dawley rats were treated with 1 mg mercuric chloride (HgCl2)/kg, sc 6 hr prior to or simultaneously with a single 2.5-mmole/kg ip dose of bromobenzene and sacrificed 48 hr after the bromobenzene dose, the activities of serum transaminases
K Lertratanangkoon et al.
Drug metabolism and disposition: the biological fate of chemicals, 15(6), 857-867 (1987-11-01)
Premercapturic acids derived from bromobenzene 3,4-oxide were found to act as precursors of 3- and 4-bromophenol in the rat and guinea pig. The 4-S- and 3-S- positional isomers used in this study were rat urinary metabolites and were prepared in
Girish Chandra et al.
Archives of pharmacal research, 35(4), 639-645 (2012-05-04)
An improved synthesis of DNA-dependent protein kinase inhibitor, IC86621 is described. This developed method provides an easy access to this simple molecule by using amination, acetylation and Fries rearrangement reactions.
R G Schnellmann et al.
The Journal of pharmacology and experimental therapeutics, 237(2), 456-461 (1986-05-01)
An in vitro model using a suspension of rabbit renal proximal tubules was developed to investigate the mechanism of nephrotoxicity of bromobenzene. Using oxygen consumption, glutathione concentrations and retention of lactate dehydrogenase activity as markers of toxicity, the rank order
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