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About This Item
线性分子式:
BrC6H4CH2OH
CAS号:
分子量:
187.03
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22
推荐产品
化驗
99%
形狀
liquid
折射率
n20/D 1.584 (lit.)
bp
165 °C/16 mmHg (lit.)
密度
1.56 g/mL at 25 °C (lit.)
官能基
bromo
hydroxyl
SMILES 字串
OCc1cccc(Br)c1
InChI
1S/C7H7BrO/c8-7-3-1-2-6(4-7)5-9/h1-4,9H,5H2
InChI 密鑰
FSWNRRSWFBXQCL-UHFFFAOYSA-N
應用
3-Bromobenzyl alcohol was employed in the preparation of tert-butyl 3-(3-bromophenyl)-2-cyanopropanoate and silyl ether.
儲存類別代碼
10 - Combustible liquids
水污染物質分類（WGK）
WGK 3
閃點（°F）
Not applicable
閃點（°C）
Not applicable
個人防護裝備
Eyeshields, Gloves
其他客户在看
Rocky J Barney et al.
Bioorganic & medicinal chemistry, 18(20), 7212-7220 (2010-09-14)
Geminal bisphosphonates display varied biological activity depending on the nature of the substituents on the central carbon atom. For example, the nitrogenous bisphosphonates zoledronate and risedronate inhibit the enzyme farnesyl diphosphate synthase while digeranyl bisphosphonate has been shown to inhibit
Iridium catalysed alkylation of 4-hydroxy coumarin, 4-hydroxy-2-quinolones and quinolin-4 (1H)-one with alcohols under solvent free thermal conditions.
Grigg R, et al.
Tetrahedron, 65(36), 7468-7473 (2009)
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