123838
4-联苯甲醇
98%
别名:
4-(羟甲基)联苯, 4-苯基苄醇
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关于此项目
线性分子式:
C6H5C6H4CH2OH
化学文摘社编号:
分子量:
184.23
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
222-745-2
Beilstein/REAXYS Number:
1937761
MDL number:
产品名称
4-联苯甲醇, 98%
InChI key
AXCHZLOJGKSWLV-UHFFFAOYSA-N
InChI
1S/C13H12O/c14-10-11-6-8-13(9-7-11)12-4-2-1-3-5-12/h1-9,14H,10H2
SMILES string
OCc1ccc(cc1)-c2ccccc2
assay
98%
mp
96-100 °C (lit.)
solubility
acetone: soluble 25 mg/mL
functional group
hydroxyl
phenyl
Quality Level
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Application
联苯-4-甲醇可用作快速定量测定烷基锂的试剂。
General description
联苯-4-甲醇在 CH3SO3H 催化的碳酸亚丙酯（TMC）的开环聚合以及 ε-己内酯和 TMC 的共聚过程中充当单官能醇引发剂。
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
A New Insight Into the Mechanism of the Ring-Opening Polymerization of Trimethylene Carbonate Catalyzed by Methanesulfonic Acid.
Campos JM, et al.
Macromolecular Chemistry and Physics, 214(1), 85-93 (2013)
The Journal of Organic Chemistry, 48, 2603-2603 (1983)
DNA damage and its repair in cultured human alveolar tumor cells treated with benzyl chloride, 4-chloromethylbiphenyl or 4-hydroxymethylbiphenyl.
R Mirzayans et al.
Mutation research, 100(1-4), 203-206 (1982-01-01)
UKEMS trial compounds: induction of unscheduled DNA synthesis in HeLa S3 cells.
R H Barrett
Mutation research, 100(1-4), 207-209 (1982-01-01)
Transformation of BHK 21 C13 cells by BC, 4CMB and 4HMB using the method of Styles.
A Poole et al.
Mutation research, 100(1-4), 215-217 (1982-01-01)
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