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Merck
CN

131482

4-苯基-3-氨基硫脲

99%

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关于此项目

线性分子式:
C6H5NHCSNHNH2
化学文摘社编号:
分子量:
167.23
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
226-329-1
Beilstein/REAXYS Number:
608285
MDL number:
Assay:
99%
Form:
solid
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Quality Level

assay

99%

form

solid

mp

138-140 °C (lit.)

functional group

amine, hydrazine, thiourea

SMILES string

NNC(=S)Nc1ccccc1

InChI

1S/C7H9N3S/c8-10-7(11)9-6-4-2-1-3-5-6/h1-5H,8H2,(H2,9,10,11)

InChI key

KKIGUVBJOHCXSP-UHFFFAOYSA-N

Application

4-Phenylthiosemicarbazide was used in the synthesis of amberlite XAD resins. It was also used in the synthesis of a series of thiosemicarbazones.


pictograms

Skull and crossbones

signalword

Danger

hcodes

Hazard Classifications

Acute Tox. 2 Oral

存储类别

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

法规信息

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分析证书(COA)

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Justin W Hicks et al.
Chemistry & biodiversity, 5(11), 2415-2422 (2008-11-28)
Addition of thiosemicarbazide, 4-allylthiosemicarbazide, and 4-phenylthiosemicarbazide to (formylphenyl)boronic acids affords a series of thiosemicarbazones containing boronic acids. Addition of 2-formylphenylboronic acid to the thiosemicarbazides gave the corresponding cyclic 2,3,1-benzodiazaborines. All new compounds have been investigated for potential antifungal activity.
Derya Kara et al.
Journal of hazardous materials, 165(1-3), 1165-1169 (2008-12-17)
A matrix separation and analyte preconcentration system using Amberlite XAD copolymer resins functionalized by Schiff base reactions coupled with atomic spectrometry has been developed. Three different functionalized Amberlite XAD resins were synthesized using 4-phenylthiosemicarbazide, 2,3-dihydroxybenzaldehyde and 2-thiophenecarboxaldehyde as reagents. These



全球贸易项目编号

货号GTIN
131482-50G04061838728401
131482-10G04061838728395