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4-[3,5-BIS(TRIFLUOROMETHYL)PHENYL]-3-THIOSEMICARBAZIDE is a thiosemicarbazide derivative with the molecular formula C9H5F6N3S. It features a phenyl ring substituted with two trifluoromethyl groups, which contributes to its unique chemical properties. 4-[3,5-BIS(TRIFLUOROMETHYL)PHENYL]-3-THIOSEMICARBAZIDE has potential applications in medicinal chemistry due to its ability to form complexes with transition metal ions, which may exhibit biological activity.

38901-31-4

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38901-31-4 Usage

Uses

Used in Medicinal Chemistry:
4-[3,5-BIS(TRIFLUOROMETHYL)PHENYL]-3-THIOSEMICARBAZIDE is used as a complexing agent for transition metal ions in medicinal chemistry. Its ability to form complexes with these metal ions may result in biological activity, making it a promising candidate for drug development.
Used in Antimicrobial Applications:
4-[3,5-BIS(TRIFLUOROMETHYL)PHENYL]-3-THIOSEMICARBAZIDE is used as an antimicrobial agent due to its thiosemicarbazide structure, which is known to exhibit antimicrobial properties. This makes it a potential candidate for the development of new antimicrobial drugs to combat resistant bacteria.
Used in Antifungal Applications:
4-[3,5-BIS(TRIFLUOROMETHYL)PHENYL]-3-THIOSEMICARBAZIDE is used as an antifungal agent, leveraging its thiosemicarbazide properties to target and inhibit fungal growth. This application can contribute to the development of new antifungal drugs to treat various fungal infections.
Used in Antitumor Applications:
4-[3,5-BIS(TRIFLUOROMETHYL)PHENYL]-3-THIOSEMICARBAZIDE is used as an antitumor agent in the field of oncology. Its thiosemicarbazide structure is known to exhibit antitumor properties, making it a potential candidate for the development of new cancer treatments.
Used in Drug Development Research:
4-[3,5-BIS(TRIFLUOROMETHYL)PHENYL]-3-THIOSEMICARBAZIDE is used as a subject of research in drug development. Its unique structure and potential biological activity make it an interesting compound for further investigation into its therapeutic potential across various medical fields.

Check Digit Verification of cas no

The CAS Registry Mumber 38901-31-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,9,0 and 1 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 38901-31:
(7*3)+(6*8)+(5*9)+(4*0)+(3*1)+(2*3)+(1*1)=124
124 % 10 = 4
So 38901-31-4 is a valid CAS Registry Number.

38901-31-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[3,5-Di(trifluoromethyl)phenyl]-3-thiosemicarbazide

1.2 Other means of identification

Product number -
Other names 1-amino-3-[3,5-bis(trifluoromethyl)phenyl]thiourea

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:38901-31-4 SDS

38901-31-4Downstream Products

38901-31-4Relevant articles and documents

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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