131482

Sigma-Aldrich

4-Phenylthiosemicarbazide

99%

Linear Formula:
C6H5NHCSNHNH2
CAS Number:
Molecular Weight:
167.23
Beilstein/REAXYS Number:
608285
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22
Pricing and availability is not currently available.

Quality Level

assay

99%

mp

138-140 °C (lit.)

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

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Related Categories

Application

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

Packaging

10, 50 g in glass bottle

Pictograms

Skull and crossbones

Signal Word

Danger

Hazard Statements

Precautionary Statements

Personal Protective Equipment

dust mask type N95 (US),Eyeshields,Gloves

RIDADR

UN 2811 6.1 / PGII

WGK Germany

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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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