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Merck

101079

Sigma-Aldrich

3-溴苯酚

98%

别名:

m-Bromophenol

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About This Item

线性分子式:
BrC6H4OH
CAS号:
分子量:
173.01
Beilstein:
1853950
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

品質等級

化驗

98%

形狀

solid

bp

236 °C (lit.)

mp

28-32 °C (lit.)

官能基

bromo

SMILES 字串

Oc1cccc(Br)c1

InChI

1S/C6H5BrO/c7-5-2-1-3-6(8)4-5/h1-4,8H

InChI 密鑰

MNOJRWOWILAHAV-UHFFFAOYSA-N

基因資訊

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一般說明

3-溴苯酚用于suzuki-miyaura偶联反应,以及合成五环合成砌块苯并苯二苯并呋喃。

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

No data available

閃點(°C)

No data available

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


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分析证书(COA)

Lot/Batch Number

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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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