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Merck
CN

148229

Thiobenzamide

98%

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About This Item

Linear Formula:
C6H5CSNH2
CAS Number:
Molecular Weight:
137.20
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
218-765-6
Beilstein/REAXYS Number:
606021
MDL number:
Assay:
98%
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assay

98%

mp

113-117 °C (lit.)

functional group

amine, phenyl

SMILES string

NC(=S)c1ccccc1

InChI

1S/C7H7NS/c8-7(9)6-4-2-1-3-5-6/h1-5H,(H2,8,9)

InChI key

QIOZLISABUUKJY-UHFFFAOYSA-N

Application

Thiobenzamide was used to prepare amide and amidine adducts. It was also used in the synthesis of 4-oxo-4H-chromene-3-carbothioic acid N-phenylamides.


pictograms

Skull and crossbones

signalword

Danger

hcodes

Hazard Classifications

Acute Tox. 3 Oral

Storage Class

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

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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



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P Joseph et al.
Placenta, 14(3), 309-319 (1993-05-01)
Human term placental peroxidase [donor: hydrogen peroxide (H2O2) oxidoreductase] from non-smoking women was purified by extraction of the membrane fraction with 0.5 M Ca2+ followed by affinity chromatography on concanavalin A, hydrophobic chromatography on phenyl sepharose CL-4B and gel filtration
A Kubo et al.
Archives of biochemistry and biophysics, 345(2), 271-277 (1997-10-06)
The flavin-containing monooxygenases (FMOs) are a family of flavoenzymes and contain one molecule of FAD per monomer. In order to demonstrate where FMO interacts with FAD, four mutants for the rat liver FMO1 protein were expressed in yeast and characterized.
Chemical Research in Toxicology. In this issue.
Chemical research in toxicology, 21(7), 1320-1321 (2008-07-22)



Global Trade Item Number

SKUGTIN
148229-50G04061833544587
148229-10G04061838737908