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关于此项目
经验公式(希尔记法):
C17H12O
化学文摘社编号:
分子量:
232.28
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
98%
Form:
solid
InChI
1S/C17H12O/c18-10-14-7-6-13-5-4-11-2-1-3-12-8-9-15(14)17(13)16(11)12/h1-9,18H,10H2
SMILES string
OCc1ccc2ccc3cccc4ccc1c2c34
InChI key
NGDMLQSGYUCLDC-UHFFFAOYSA-N
assay
98%
form
solid
mp
123-126 °C (lit.)
functional group
hydroxyl
Quality Level
Application
1-芘乙醇可用于:
- 合成腺苷-5′ 的钳形苯桥接荧光选择性传感器-三磷酸盐 (ATP) 检测。
- 作为合成芘端聚甲基丙烯酸缩水甘油酯聚合物的起始原料。
- 作为合成芘核心星形聚合物的引发剂。
- 合成医药和农药领域的重要中间体 1-芘甲醛。
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)
Walter Meinl et al.
Pharmacogenetics, 12(9), 677-689 (2002-12-05)
Various enzymatically formed sulfuric acid esters are chemically reactive and mutagenic. This metabolic activation pathway is not detected in standard in-vitro mutagenicity test systems. We describe the construction of Salmonella typhimurium TA1538-derived strains expressing alloenzymes *1, *2, *3, *5, *6
Highly efficient oxidation of alcohols to carbonyl compounds in the presence of molecular oxygen using a novel heterogeneous ruthenium catalyst.
Ji H, et al.
Tetrahedron Letters, 43(40), 7179-7183 (2002)
Y J Surh et al.
Carcinogenesis, 11(9), 1451-1460 (1990-09-01)
Our previous studies on 7-hydroxymethyl-12-methylbenz[a]anthracene and 6-hydroxymethylbenzo[a]pyrene showed that cytosolic sulfotransferase activity plays a major role in the formation of hepatic benzylic DNA and RNA adducts by these carcinogens in rats. In the present study, we found similar sulfotransferase activity
H Glatt et al.
Carcinogenesis, 14(4), 599-602 (1993-04-01)
1-Hydroxymethylpyrene (HMP), a primary benzylic alcohol, and 4H-cyclopenta[def]chrysen-4-ol (OH-CPC), a secondary benzylic alcohol, were investigated for mutagenicity in Salmonella typhimurium (reversion of the his- strain TA98) in the presence of various xenobiotic-metabolizing systems. In the direct test, HMP was inactive
Encapsulation of functional moieties within branched star polymers: effect of chain length and solvent on site isolation.
Hecht S, et al.
Journal of the American Chemical Society, 123(1), 18-25 (2001)
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