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Merck
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Key Documents

Altri documenti

P39605

Sigma-Aldrich

Phthalide

98%

Sinonimo/i:

1-Isobenzofuranone

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About This Item

Formula empirica (notazione di Hill):
C8H6O2
Numero CAS:
87-41-2
Peso molecolare:
134.13
Beilstein:
114632
Numero CE:
201-744-0
Numero MDL:
MFCD00005906
Codice UNSPSC:
12352100
ID PubChem:
24898475
NACRES:
NA.22

Livello qualitativo

100

Saggio

98%

Forma fisica

powder

P. eboll.

290 °C (lit.)

Punto di fusione

71-74 °C (lit.)

Stringa SMILE

O=C1OCc2ccccc12

InChI

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

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Categorie correlate

Codice della classe di stoccaggio

13 - Non Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

305.6 °F - closed cup

Punto d’infiammabilità (°C)

152 °C - closed cup

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

Certificati d'analisi (COA)

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3-N-Butylphthalide ≥98% (HPLC)

Sigma-Aldrich

SMB00312

3-N-Butylphthalide

1,2-Benzenedimethanol 97%

Sigma-Aldrich

184829

1,2-Benzenedimethanol

Isochroman 99%

Sigma-Aldrich

I15807

Isochroman

5-Bromophthalide 97%

Sigma-Aldrich

647187

5-Bromophthalide

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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