389439
1-芘甲醇
98%
别名:
1-羟甲基芘, 1-（1-羟甲基）芘
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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:
产品名称
1-芘甲醇, 98%
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)
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.
Chemico-biological interactions, 92(1-3), 305-319 (1994-06-01)
1-Hydroxymethylpyrene (HMP) is activated to a potent mutagen, detectable in Salmonella typhimurium, in the presence of hepatic cytosol, cofactor for sulfotransferases, and chloride anions. The number of induced mutations is linear to the amount of cytosol used over a wide
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)
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
H Glatt et al.
Chemico-biological interactions, 109(1-3), 195-219 (1998-05-05)
Sulfation is a common final step in the biotransformation of xenobiotics and is traditionally associated with inactivation. However, the sulfate group is electron-withdrawing and may be cleaved off heterolytically in some molecules leading to electrophilic cations which may form adducts
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