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N-methyl-2-phenylhydrazinecarbothioamide, also known as phenylhydrazinecarbothioamide, is a chemical compound with the molecular formula C9H11N3S. It is a thioamide derivative of phenylhydrazine, which is a substituted hydrazine commonly used in organic synthesis. N-methyl-2-phenylhydrazinecarbothioamide has been studied for its potential use in pharmaceutical and agricultural applications, particularly as a potential insecticide.

13207-50-6

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13207-50-6 Usage

Uses

Used in Pharmaceutical Applications:
N-methyl-2-phenylhydrazinecarbothioamide is used as a pharmaceutical intermediate for the synthesis of various therapeutic agents. Its unique chemical structure allows it to be a versatile building block in the development of new drugs with potential applications in treating various diseases.
Used in Agricultural Applications:
N-methyl-2-phenylhydrazinecarbothioamide is used as a potential insecticide in the agricultural industry. Its insecticidal properties make it a candidate for controlling pests and protecting crops from damage. N-methyl-2-phenylhydrazinecarbothioamide's effectiveness in targeting specific pests without causing harm to beneficial organisms or the environment is being investigated.
Used in Organic Synthesis:
N-methyl-2-phenylhydrazinecarbothioamide is used as a key intermediate in the synthesis of various organic compounds. Its reactivity and functional groups make it a valuable component in the preparation of complex organic molecules, which can be used in a wide range of applications, including pharmaceuticals, agrochemicals, and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 13207-50-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,0 and 7 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 13207-50:
(7*1)+(6*3)+(5*2)+(4*0)+(3*7)+(2*5)+(1*0)=66
66 % 10 = 6
So 13207-50-6 is a valid CAS Registry Number.

13207-50-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-anilino-3-methylthiourea

1.2 Other means of identification

Product number -
Other names 1-phenyl-4-methyl-3-thiosemicarbazide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:13207-50-6 SDS

13207-50-6Relevant academic research and scientific papers

Synthesis and multinuclear NMR investigation of some mesoionic 3-phenyl-5-imino-1,2,3,4-oxatriazole imines

Ja?wiński, Jaros?aw,Staszewska-Krajewska, Olga

, p. 23 - 33 (2007/10/03)

Six new derivatives of mesoionic 3-phenyl-5-imino-1,2,3,4-oxatriazole imine have been obtained and investigated by 1H, 13C, 14N, 15N and 17O NMR techniques. The 15N and 17O NMR s

Antiimplantation Agents: Part I - 1-Arylthiosemicarbazides

Nagarajan, K.,Talwalker, P.K.,Kulkarni, C.L.,Venkateswarlu, A.,Prabhu, S.S.,Nayak, G.V.

, p. 1243 - 1257 (2007/10/02)

Several 1-arylthiosemicarbazides, 2-arylhydrazinothiazolines and 2-arylhydrazinodihydrothiazines have been examined for their antiimplantation activity in rats.Among the active compounds, 4-methyl-1-(3,5-bistrifluoromethylphenyl)thiosemicarbazide (3, C 2696-Go) and the corresponding 4,4-dimethyl (47), ethyl (4), n-butyl (5) and allyl (6) derivatives completely inhibit implantation at doses 10, 3, 20, 20 and 30 mg/kg respectively.The 3,4-dichlorophenyl analogue (32) is effective at a dose of 30 mg/kg. 2-(3,5-Bistrifluoromethylphenyl)hydrazinothiazoline (51) and the corresponding dihydrothiazine (63) show a weaker activity.The biological profile of C 2696-Go has been investigated in detail.It appears to prevent implantation by its antiuterotropic activity and ability to inhibit desiduoma formation.

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