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Merck
CN

65357

4-甲氧基苯硫酚

purum, ≥98.0% (GC)

别名:

4-甲氧基硫代苯酚, 对甲氧基苯硫酚

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线性分子式:
CH3OC6H4SH
化学文摘社编号:
分子量:
140.20
EC Number:
211-799-2
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
1446910
MDL number:
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grade

purum

assay

≥98.0% (GC)

refractive index

n20/D 1.5831 (lit.), n20/D 1.584

bp

100-103 °C/13 mmHg (lit.)

density

1.14 g/mL at 25 °C (lit.)

SMILES string

COc1ccc(S)cc1

InChI

1S/C7H8OS/c1-8-6-2-4-7(9)5-3-6/h2-5,9H,1H3

InChI key

NIFAOMSJMGEFTQ-UHFFFAOYSA-N

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

10 - Combustible liquids

wgk

WGK 3

flash_point_f

204.8 °F - closed cup

flash_point_c

96 °C - closed cup

ppe

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

法规信息

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分析证书(COA)

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Hadeel T Al-Sinjilawi et al.
Archiv der Pharmazie, 347(11), 861-872 (2014-09-16)
A series of substituted 4-oxopyrido[2,3-a]phenothiazine-3-carboxylic acids (6a-d) were prepared via cyclization of the corresponding ethyl 7-(arylthioxy)-8-nitro(or azido)-4-oxoquinoline-3-carboxylates (3a-d/4a-d), followed by hydrolysis of the resultant esters (5a-d). Among these tetracyclics, compound 6a with unsubstituted terminal benzo-ring D was the most active

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