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P39605

Sigma-Aldrich

Phthalid

98%

Synonym(e):

1-Isobenzofuranon

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About This Item

Empirische Formel (Hill-System):
C8H6O2
CAS-Nummer:
87-41-2
Molekulargewicht:
134.13
Beilstein:
114632
EG-Nummer:
201-744-0
MDL-Nummer:
MFCD00005906
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24898475
NACRES:
NA.22

Qualitätsniveau

100

Assay

98%

Form

powder

bp

290 °C (lit.)

mp (Schmelzpunkt)

71-74 °C (lit.)

SMILES String

O=C1OCc2ccccc12

InChI

1S/C8H6O2/c9-8-7-4-2-1-3-6(7)5-10-8/h1-4H,5H2

InChIKey

WNZQDUSMALZDQF-UHFFFAOYSA-N

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Verwandte Kategorien

Lagerklassenschlüssel

13 - Non Combustible Solids

WGK

WGK 1

Flammpunkt (°F)

305.6 °F - closed cup

Flammpunkt (°C)

152 °C - closed cup

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves

Analysenzertifikate (COA)

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3-N-Butylphthalide ≥98% (HPLC)

Sigma-Aldrich

SMB00312

3-N-Butylphthalide

1,2-Benzoldimethanol 97%

Sigma-Aldrich

184829

1,2-Benzoldimethanol

Isochroman 99%

Sigma-Aldrich

I15807

Isochroman

5-Bromphthalid 97%

Sigma-Aldrich

647187

5-Bromphthalid

Ligustilide ≥96% (HPLC)

Sigma-Aldrich

SMB00400

Ligustilide

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
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
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
Chang-Yin Li et al.
Journal of pharmaceutical and biomedical analysis, 55(1), 146-160 (2011-02-01)
In this work, the metabolite profiles of Danggui Buxue Tang (DBT) in rat bile and plasma were qualitatively described, and the possible metabolic pathways of DBT were subsequently proposed. Emphasis was put on correlative analysis of metabolite profiling in different
Song-Hwa Chae et al.
Journal of agricultural and food chemistry, 59(15), 8193-8198 (2011-07-07)
The residual contact toxicity of three benzofuranoids (Z)-butylidenephthalide (1), (3S)-butylphthalide (2), and (Z)-ligustilide (3) identified in the rhizome of Cnidium officinale (Apiaceae) to B- and Q-biotype females of Bemisia tabaci was evaluated using a leaf-dip bioassay. Results were compared with
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