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(1H-benzimidazol-2-ylsulfanyl)acetic acid benzylidene hydrazide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

30065-38-4

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30065-38-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30065-38-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,0,6 and 5 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 30065-38:
(7*3)+(6*0)+(5*0)+(4*6)+(3*5)+(2*3)+(1*8)=74
74 % 10 = 4
So 30065-38-4 is a valid CAS Registry Number.

30065-38-4Downstream Products

30065-38-4Relevant academic research and scientific papers

Synthesis of some new nucleosides derived from 2-mercapto benzimidazole with expected biological activity

Amer, Hamada H.,Ali, Omar M.,El-Kafaween, Ibrahim Kh.

, p. 2303 - 2310 (2017/11/15)

2-mercaptobenzimidazole derivatives and their acyclic nucleosides were synthesized. The synthesized compounds were tested for their antibacterial activity against Escherichia coli, Staphylococcus aureus and S. epidermidis. Most of tested compounds showed

Synthesis of 2-mercaptobenzimidazole derivatives as potential anti-microbial and cytotoxic agents

Hosamani, Kallappa M.,Shingalapur, Ramya V.

, p. 311 - 319 (2011/11/05)

A series of novel 2-(1H-benzimidazol-2-ylsulfanyl)-N-(4-oxo-2-phenyl- thiazolidin-3yl)-acetamide 5a-j have been synthesized from various aldehydes and 2-(5-phenyl-[1,3,4]-oxadiazol-2-ylmethylsulfanyl)-1H-benzimidazole 6a-j from various benzoic acids. Thes

Derivatives of benzimidazole pharmacophore: Synthesis, anticonvulsant, antidiabetic and DNA cleavage studies

Shingalapur, Ramya V.,Hosamani, Kallappa M.,Keri, Rangappa S.,Hugar, Mallinath H.

experimental part, p. 1753 - 1759 (2010/06/17)

In seeking broad spectrum pharmacological activities of benzimidazole derivatives, a group of 4-thiazolidinones 5(a-j) and 1,3,4-oxadiazoles 6(a-j) containing 2-mercapto benzimidazole moiety were synthesized and screened for in vivo anticonvulsant activit

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