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Merck

519561

Sigma-Aldrich

3-溴苯甲酮

98%

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About This Item

线性分子式:
BrC6H4COC6H5
CAS号:
分子量:
261.11
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

方案

98%

mp

74.5-77.5 °C (lit.)

官能团

bromo
ketone
phenyl

SMILES字符串

Brc1cccc(c1)C(=O)c2ccccc2

InChI

1S/C13H9BrO/c14-12-8-4-7-11(9-12)13(15)10-5-2-1-3-6-10/h1-9H

InChI key

XNUMUNIJQMSNNN-UHFFFAOYSA-N

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Mark F. Mechelke et al.
The Journal of organic chemistry, 64(13), 4821-4829 (2001-10-25)
The synthesis of a family of farnesol analogues, incorporating aromatic rings, has been achieved in high yields through the development of a regioselective coupling of allylic tetrahydropyranyl ethers with organometallic reagents. The allylic THP group is displaced readily by Grignard
Sonovoltammetric measurement of the rates of electrode processes with fast coupled homogeneous kinetics: Making macroelectrodes behave like microelectrodes.
Compton RG, et al.
Chemical Communications (Cambridge, England), 9, 1017-1018 (1996)
Transition-metal catalyzed synthesis of ketoprofen.
Ramminger C, et al.
Journal of the Brazilian Chemical Society, 11(2), 105-111 (2000)
Similar or Totally Different: The Control of Conjugation Degree through Minor Structural Modifications, and Deep-Blue Aggregation-Induced Emission Luminogens for Non-Doped OLEDs.
Huang J, et al.
Advances in Functional Materials, 23(18), 2329-2337 (2013)

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