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2H-Benzimidazole-2-thione,1,3-dihydro-1-propyl-(9CI) is an organic heterocyclic compound that features a benzimidazole ring with a thione functional group and a 1,3-dihydro-1-propyl substituent. It belongs to the class of benzimidazole derivatives, which have been recognized for their diverse biological activities.

67624-25-3

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67624-25-3 Usage

Uses

Used in Pharmaceutical Industry:
2H-Benzimidazole-2-thione,1,3-dihydro-1-propyl-(9CI) is used as a potential pharmaceutical agent for its possible antimicrobial, antiviral, and antitumor properties. 2H-Benzimidazole-2-thione,1,3-dihydro-1-propyl-(9CI)'s unique structure and functional groups may contribute to its therapeutic effects, making it a candidate for further research and development in the medical field.
Further research and testing are necessary to fully understand the potential applications and benefits of 2H-Benzimidazole-2-thione,1,3-dihydro-1-propyl-(9CI) in various industries, particularly in the pharmaceutical sector.

Check Digit Verification of cas no

The CAS Registry Mumber 67624-25-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,6,2 and 4 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 67624-25:
(7*6)+(6*7)+(5*6)+(4*2)+(3*4)+(2*2)+(1*5)=143
143 % 10 = 3
So 67624-25-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H12N2S/c1-2-7-12-9-6-4-3-5-8(9)11-10(12)13/h3-6H,2,7H2,1H3,(H,11,13)

67624-25-3SDS

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 3-propyl-1H-benzimidazole-2-thione

1.2 Other means of identification

Product number -
Other names 1-Propyl-1H-benzoimidazole-2-thiol

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:67624-25-3 SDS

67624-25-3Downstream Products

67624-25-3Relevant academic research and scientific papers

Synthesis of N-substituted benzimidazole-2-thiones

Doerge,Cooray

, p. 1789 - 1795 (2007/10/02)

General methods were developed for N-substitution of benzimidazoline-2-thione with alkyl, alkenyl, alkynyl and acyl groups using S-tritylation as a protecting reaction.

A Facile One Pot Synthesis of 1-Alkylbenzimidazoline-2-thiones

Lee, Tae Ryong,Kim, Kyongtae

, p. 747 - 751 (2007/10/02)

Reactions of benzimidazoline-2-thione with alkyl halides in the presence of sodium naphthalenide in tetrahydrofuran at room temperature under a nitrogen atmosphere afforded 1-alkyl-2-alkylthiobenzimidazoles in excellent yields, which underwent a bond cleavage between S and C of alkyl group to give excellent yields of 1-alkylbenzimidazoline-2-thiones by the treatment with an additional amount of sodium naphthalenide.

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