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4-(3-Methoxypropyl)-3-thiosemicarbazide is a chemical compound with the molecular formula C6H14N4OS. It is a thiosemicarbazide derivative that features a thiol group and a propyl chain with a methoxy group attached to it. 4-(3-METHOXYPROPYL)-3-THIOSEMICARBAZIDE is recognized for its potential as a versatile building block in organic synthesis and pharmaceutical research, particularly for the preparation of various heterocyclic compounds. Its thiosemicarbazide moiety also exhibits biological activities, including antibacterial and antifungal properties, which make it a promising candidate for the development of new antimicrobial agents.

71058-32-7

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71058-32-7 Usage

Uses

Used in Organic Synthesis:
4-(3-Methoxypropyl)-3-thiosemicarbazide is used as a versatile building block in organic synthesis for the preparation of various heterocyclic compounds. Its unique structure allows for the creation of a wide range of chemical entities, making it valuable in the development of novel pharmaceuticals and other organic compounds.
Used in Pharmaceutical Research:
In pharmaceutical research, 4-(3-Methoxypropyl)-3-thiosemicarbazide is utilized as a key intermediate for the synthesis of therapeutic agents. Its potential biological activities, including its ability to inhibit bacterial and fungal growth, make it a candidate for the development of new antimicrobial drugs, addressing the need for novel treatments in the face of increasing antibiotic resistance.
Used in Medicinal Chemistry Studies:
4-(3-Methoxypropyl)-3-thiosemicarbazide is employed in medicinal chemistry studies to explore its potential as a precursor for the development of new pharmaceuticals. Its thiosemicarbazide moiety, which has demonstrated biological activity, is of particular interest for the design and synthesis of compounds with therapeutic potential.
Used in Antimicrobial Agent Development:
Due to its antibacterial and antifungal properties, 4-(3-Methoxypropyl)-3-thiosemicarbazide is used as a potential candidate for the development of new antimicrobial agents. This is crucial in the ongoing battle against drug-resistant infections, where novel agents are needed to combat a wide range of pathogens.

Check Digit Verification of cas no

The CAS Registry Mumber 71058-32-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,0,5 and 8 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 71058-32:
(7*7)+(6*1)+(5*0)+(4*5)+(3*8)+(2*3)+(1*2)=107
107 % 10 = 7
So 71058-32-7 is a valid CAS Registry Number.
InChI:InChI=1/C5H13N3OS/c1-9-4-2-3-7-5(10)8-6/h2-4,6H2,1H3,(H2,7,8,10)

71058-32-7SDS

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 1-amino-3-(3-methoxypropyl)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

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More Details:71058-32-7 SDS

71058-32-7Upstream product

71058-32-7Relevant academic research and scientific papers

Synthesis and SAR of novel conformationally restricted oxazolidinones possessing Gram-positive and fastidious Gram-negative antibacterial activity. Part 2: Amino substitutions on heterocyclic D-ring system

Choy, Allison L.,Vara Prasad,Boyer, Frederick E.,Huband, Michael D.,Dermyer, Michael R.

, p. 4699 - 4702 (2007)

A novel series of conformationally restricted oxazolidinones was synthesized, in which the heterocyclic D ring was substituted with various amino groups. Several analogs exhibited potent activity against both Gram-positive and fastidious Gram-negative org

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