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
产品名称
4-苯基-3-氨基硫脲, 99%
InChI key
KKIGUVBJOHCXSP-UHFFFAOYSA-N
InChI
1S/C7H9N3S/c8-10-7(11)9-6-4-2-1-3-5-6/h1-5H,8H2,(H2,9,10,11)
SMILES string
NNC(=S)Nc1ccccc1
assay
99%
form
solid
mp
138-140 °C (lit.)
functional group
amine
hydrazine
thiourea
Quality Level
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Application
4-Phenylthiosemicarbazide was used in the synthesis of amberlite XAD resins. It was also used in the synthesis of a series of thiosemicarbazones.
signalword
Danger
hcodes
pcodes
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
新产品
此项目有
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
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