Welcome to LookChem.com Sign In|Join Free
  • or
N-(3,4-Dimethylphenyl)hydrazinecarbothioamide is a chemical compound characterized by the molecular formula C9H12N4S. It is a hydrazine derivative, featuring a hydrazine group (-NHNH2) attached to a carbon atom within a carbothioamide group (-C(=S)NHR). The incorporation of a dimethylphenyl group endows the molecule with distinct chemical and physical attributes that can be advantageous for specific applications. N-(3,4-DIMETHYLPHENYL)HYDRAZINECARBOTHIOAMIDE plays a role in organic synthesis and medicinal chemistry, often serving as a reagent or a building block for the creation of a diverse array of compounds. Its unique structure and properties render it a candidate for potential uses in pharmaceutical research, material science, and other related fields.

6610-33-9

Post Buying Request

6610-33-9 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

6610-33-9 Usage

Uses

Used in Organic Synthesis:
N-(3,4-Dimethylphenyl)hydrazinecarbothioamide is utilized as a reagent in organic synthesis for its ability to contribute to the formation of various complex organic compounds. Its presence can influence the reactivity and selectivity of reactions, making it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, N-(3,4-Dimethylphenyl)hydrazinecarbothioamide serves as a building block for the development of new pharmaceutical agents. Its unique structure allows it to be a part of the molecular framework of potential drug candidates, contributing to their biological activity and pharmacological properties.
Used in Pharmaceutical Research:
Due to its distinctive chemical features, N-(3,4-Dimethylphenyl)hydrazinecarbothioamide may be explored in pharmaceutical research for its potential to contribute to the discovery and design of novel therapeutic agents. Its incorporation into drug molecules could lead to new treatments for various diseases and medical conditions.
Used in Material Science:
N-(3,4-DIMETHYLPHENYL)HYDRAZINECARBOTHIOAMIDE's properties may also find applications in material science, where it could be employed to develop new materials with specific characteristics. Its use in this field could lead to advancements in areas such as polymer science, nanotechnology, and the creation of functional materials with tailored properties for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 6610-33-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,1 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6610-33:
(6*6)+(5*6)+(4*1)+(3*0)+(2*3)+(1*3)=79
79 % 10 = 9
So 6610-33-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H13N3S/c1-6-3-4-8(5-7(6)2)11-9(13)12-10/h3-5H,10H2,1-2H3,(H2,11,12,13)

6610-33-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-amino-3-(3,4-dimethylphenyl)thiourea

1.2 Other means of identification

Product number -
Other names -

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:6610-33-9 SDS

6610-33-9Relevant academic research and scientific papers

Synthesis and biological activities of novel artemisinin derivatives as cysteine protease falcipain-2 inhibitors

Liu, Yang,Lu, Wei-Qiang,Cui, Kun-Qiang,Luo, Wei,Wang, Jian,Guo, Chun

, p. 1525 - 1531 (2013/03/14)

A series of novel artemisinin derivatives were synthesized from artemisinin and different anilines. All compounds were obtained as β-isomers. The target compounds were evaluated for inhibition activity against Plasmodium falciparum falcipain-2 in vitro, and most of them exhibited potent inhibition in the low micromolar range and proved to be new types of falcipain-2 inhibitors.

Synthesis and structure-activity evaluation of isatin-β- thiosemicarbazones with improved selective activity toward multidrug-resistant cells expressing P-glycoprotein

Hall, Matthew D.,Brimacombe, Kyle R.,Varonka, Matthew S.,Pluchino, Kristen M.,Monda, Julie K.,Li, Jiayang,Walsh, Martin J.,Boxer, Matthew B.,Warren, Timothy H.,Fales, Henry M.,Gottesman, Michael M.

experimental part, p. 5878 - 5889 (2011/10/08)

Cancer multidrug resistance (MDR) mediated by ATP-binding cassette (ABC) transporters presents a significant unresolved clinical challenge. One strategy to resolve MDR is to develop compounds that selectively kill cells overexpressing the efflux transport

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 6610-33-9