4-Phenylthiosemicarbazide

Base Information

Chemical Name:4-Phenylthiosemicarbazide
CAS No.:5351-69-9
Molecular Formula:C7H9 N3 S
Molecular Weight:167.235
Hs Code.:2930909090
European Community (EC) Number:226-329-1
NSC Number:58946,704
UNII:RBH3R5JE2H
DSSTox Substance ID:DTXSID6063808
Nikkaji Number:J54.314D
Wikipedia:4-Phenylthiosemicarbazide
Wikidata:Q258799
ChEMBL ID:CHEMBL4521724
Mol file:5351-69-9.mol

Synonyms:5351-69-9;4-Phenyl-3-thiosemicarbazide;4-PHENYLTHIOSEMICARBAZIDE;N-Phenylhydrazinecarbothioamide;Hydrazinecarbothioamide, N-phenyl-;1-amino-3-phenylthiourea;Phenyl thiosemicarbazide;4-(Phenyl)thiosemicarbazide;Semicarbazide, 4-phenyl-3-thio-;3-amino-1-phenylthiourea;USAF EL-45;USAF EK-5426;NSC 704;n-phenylthiosemicarbazide;EINECS 226-329-1;NSC 58946;RBH3R5JE2H;AI3-00706;NSC-704;MFCD00007615;NSC-58946;WLN: ZMYUS&MR;4-Phenyl-3-thiosemicarbbazide;hydrazino(phenylamino)methane-1-thione;UNII-RBH3R5JE2H;4-phenyl-thiosemicarbazide;4-phenyl3-thiosemicarbazide;4phenyl-3-thiosemicarbazide;1-azanyl-3-phenyl-thiourea;4-Phenylhydrazinethiocarbamide;SCHEMBL455167;NSC704;4-Phenylthiosemicarbazide, 99%;CHEMBL4521724;DTXSID6063808;SCHEMBL21699678;N-Phenylhydrazinecarbothioamide #;HMS1784N08;N1-phenylhydrazine-1-carbothioamide;NSC58946;N-phenylhydrazinecarbimidothioic acid;STK050674;STK968645;4-PHENYL,3-THIO-SEMICARBAZIDE;AKOS000304549;AKOS002238241;AKOS022902488;BS-3911;CS-W017830;NCGC00319348-01;LS-144901;FT-0619394;P0235;EN300-16960;D91931;AB01315576-02;10.14272/KKIGUVBJOHCXSP-UHFFFAOYSA-N.1;A829648;Q258799;doi:10.14272/KKIGUVBJOHCXSP-UHFFFAOYSA-N.1;J-515938;Z56836896;F3146-4776;4-Phenylthiosemicarbazide, puriss. p.a., for spectrophotometric det. of Se, Te, >=99.0% (NT)

Suppliers and Price of 4-Phenylthiosemicarbazide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

TRC
4-Phenyl-3-thiosemicarbazide
100mg
$ 75.00

TCI Chemical
4-Phenyl-3-thiosemicarbazide >98.0%(HPLC)(T)
1g
$ 15.00

TCI Chemical
4-Phenyl-3-thiosemicarbazide >98.0%(HPLC)(T)
25g
$ 59.00

Sigma-Aldrich
4-Phenylthiosemicarbazide 99%
50g
$ 179.00

Sigma-Aldrich
4-Phenylthiosemicarbazide 99%
10g
$ 53.50

Matrix Scientific
N-Phenylhydrazinecarbothioamide
500mg
$ 126.00

Crysdot
N-Phenylhydrazinecarbothioamide 95+%
25g
$ 115.00

BLDpharm
N-Phenylhydrazinecarbothioamide 98%
1g
$ 11.00

Aronis compounds
N-phenylhydrazinecarbothioamide
20mg
$ 30.00

American Custom Chemicals Corporation
N-PHENYLHYDRAZINECARBOTHIOAMIDE 95.00%
5G
$ 1328.25

Total 57 raw suppliers

Chemical Property of 4-Phenylthiosemicarbazide

Chemical Property:

Appearance/Colour:white to slightly yellow fine crystalline powder
Vapor Pressure:0.00248mmHg at 25°C
Melting Point:138-140 °C(lit.)
Refractive Index:1.5500 (estimate)
Boiling Point:281.3°Cat760mmHg
PKA:11.01±0.70(Predicted)
Flash Point:123.9°C
PSA：82.17000
Density:1.14g/cm³
LogP:2.01090
Storage Temp.:Store at +15°C to +25°C.
Solubility.:methanol: 50 mg/mL, clear
XLogP3:0.8
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:167.05171847
Heavy Atom Count:11
Complexity:132

Purity/Quality:

97% ^*data from raw suppliers

4-Phenyl-3-thiosemicarbazide ^*data from reagent suppliers

Safty Information:

Pictogram(s): T,Xi
Hazard Codes:T,Xi
Statements: 25
Safety Statements: 45

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

Canonical SMILES:C1=CC=C(C=C1)NC(=S)NN
Uses 4-Phenylthiosemicarbazide was used in the synthesis of amberlite XAD resins. It was also used in the synthesis of a series of thiosemicarbazones.

Technology Process of 4-Phenylthiosemicarbazide

There total 31 articles about 4-Phenylthiosemicarbazide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 89.8%