W419501
苯酞
98%
别名:
2-苯并呋喃酮
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关于此项目
经验公式（希尔记法）:
C8H6O2
化学文摘社编号:
分子量:
134.13
Flavis number:
10.056
PubChem Substance ID:
UNSPSC Code:
12164502
FEMA Number:
4195
EC Number:
201-744-0
MDL number:
Beilstein/REAXYS Number:
114632
产品名称
苯酞, 98%
InChI
1S/C8H6O2/c9-8-7-4-2-1-3-6(7)5-10-8/h1-4H,5H2
InChI key
WNZQDUSMALZDQF-UHFFFAOYSA-N
SMILES string
O=C1OCc2ccccc12
biological source
synthetic
assay
98%
bp
290 °C (lit.)
mp
71-74 °C (lit.)
application(s)
flavors and fragrances
organoleptic
coconut
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存储类别
13 - Non Combustible Solids
wgk
WGK 1
flash_point_f
305.6 °F - closed cup
flash_point_c
152 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
Dario C Gerbino et al.
Organic letters, 14(9), 2338-2341 (2012-04-24)
The surprisingly facile conversion (isomerization) of 2-formyl-arylketones into 3-substituted phthalides, as observed for the marine natural product pestalone and its per-O-methylated derivative, was investigated using a series of simple 2-acylbenzaldehydes as substrates. The transformation generally proceeds smoothly in DMSO, either
Yun Wei et al.
Journal of chromatography. A, 1284, 53-58 (2013-03-15)
The phthalide compounds of Chuanxiong rhizoma including senkyunolide A, levistolide A, Z-ligustilide and 3-butylidenephthalide, have been reported as the biologically active compounds because of their therapeutic effects. In this work, online high-speed counter-current chromatography coupled with semi-preparative liquid chromatography instrument
Fangrui Zhong et al.
Journal of the American Chemical Society, 134(24), 10222-10227 (2012-05-25)
Phthalides were used for the first time in the allylic alkylation reactions with MBH carbonates for the creation of chiral 3,3-disubstituted phthalides. Highly enantioselective regiodivergent synthesis of γ-selective or β-selective allylic alkylation products was achieved by employing bifunctional chiral phosphines
Bin Xiao et al.
Bioorganic & medicinal chemistry, 20(16), 4954-4961 (2012-07-24)
On the basis of a marine fungal phthalide (paecilocin A) skeleton, we synthesized 20 analogs and evaluated them for peroxisome proliferator-activated receptor gamma (PPAR-γ) binding and activation. Among these analogs, 6 and 7 had significant PPAR-γ binding activity, and 7
Kamolchanok Tianpanich et al.
Journal of natural products, 74(1), 79-81 (2010-12-23)
Five known isocoumarins, monocerin (1), derivative 2, and fusarentin derivatives 3-5, and a new phthalide (6) were isolated from the endophytic fungus Colletotrichum sp. 2 selectively exhibited cytotoxic activity toward the HepG2 cell line. Compounds 2 and 4 scavenged 2,2-diphenyl-1-picrylhydrazyl
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