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Merck

C62794

Sigma-Aldrich

2-氯苯酚

98%

别名:

o-Chlorophenol

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About This Item

线性分子式:
ClC6H4OH
CAS号:
分子量:
128.56
Beilstein:
1905114
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

品質等級

化驗

98%

形狀

liquid

折射率

n20/D 1.558 (lit.)

bp

175-176 °C (lit.)

mp

8 °C (lit.)

密度

1.241 g/mL at 25 °C (lit.)

SMILES 字串

Oc1ccccc1Cl

InChI

1S/C6H5ClO/c7-5-3-1-2-4-6(5)8/h1-4,8H

InChI 密鑰

ISPYQTSUDJAMAB-UHFFFAOYSA-N

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應用

2-Chlorophenol is used to synthesize various organic intermediates and compounds including several polycyclic aromatic hydrocarbons and pharmacologically active molecules. It is used as a precursor to synthesize polychlorinated dibenzo p-dioxins and dibenzofurans (PCDD/Fs).

訊號詞

Danger

危險分類

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Skin Corr. 1B

儲存類別代碼

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

水污染物質分類(WGK)

WGK 2

閃點(°F)

147.2 °F - closed cup

閃點(°C)

64.0 °C - closed cup

個人防護裝備

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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Synthesis and anti-inflammatory activity evaluation of some novel 6-alkoxy (phenoxy)-[1, 2, 4] triazolo [3, 4-a] phthalazine-3-amine derivatives.
Sun, Xian-Yu et al.
European Journal of Medicinal Chemistry, 45(11), 4807-4812 (2010)
Hydroxyterphenylphoshine- Palladium Catalyst for Benzo [b] furan Synthesis from 2-Chlorophenols. Bifunctional Ligand Strategy for Cross-Coupling of Chloroarenes.
Wang, Jia-Rui and Manabe, Kei
The Journal of Organic Chemistry, 75(15), 5340-5342 (2010)
A quantum mechanical study on the formation of PCDD/Fs from 2-chlorophenol as precursor.
Zhang, Qingzhu et al.
Environmental Science & Technology, 42(19), 7301-7308 (2008)
Microwave-promoted Suzuki-Miyaura coupling of arylboronic acids with 1-bromo-2-naphthol, o-bromophenol, and o-chlorophenol.
Wawrzyniak P and Heinicke J.
Tetrahedron Letters, 47(50), 8921-8924 (2006)
Thi Thu Nga Nguyen et al.
The Journal of antimicrobial chemotherapy, 70(3), 731-738 (2014-10-23)
HIV resistance to the integrase inhibitor raltegravir in treated patients is characterized by distinct resistance pathways. We hypothesize that differences in the in vivo dynamics of HIV resistance to raltegravir are due to the genetic context of the integrase present

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