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Thibenzazoline is a chemical compound belonging to the benzazoline family, characterized by its tricyclic structure. It is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of herbicides and insecticides. The compound exhibits unique properties, such as its ability to form stable complexes with metal ions, which makes it valuable in various chemical reactions and applications. Thibenzazoline's structure and reactivity have been extensively studied, and it continues to be an important compound in the development of new chemical products and processes.

6028-35-9

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6028-35-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6028-35-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,2 and 8 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6028-35:
(6*6)+(5*0)+(4*2)+(3*8)+(2*3)+(1*5)=79
79 % 10 = 9
So 6028-35-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H10N2O2S/c12-5-10-7-3-1-2-4-8(7)11(6-13)9(10)14/h1-4,12-13H,5-6H2

6028-35-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-Bis(hydroxymethyl)-1,3-dihydro-2H-benzimidazole-2-thione

1.2 Other means of identification

Product number -
Other names 1,3-bis-hydroxymethyl-1,3-dihydro-benzimidazole-2-thione

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:6028-35-9 SDS

6028-35-9Relevant academic research and scientific papers

Application of ultrasound irradiation for the reactions of N-hydroxymethylation

Zhong,Song,Peng,Qian

, p. 3801 - 3807 (2007/10/03)

A convenient and high yield method for the N-hydroxymethylation of substituted phthalimide and benzimidazole under ultrasound irradiation is reported.

Behaviour of 2,3-dihydro-1H-benzo[d]imidazole-2-thione towards amines under Mannich-type condition

Hamama

, p. 269 - 271 (2007/10/03)

2,3-Dihydro-1H-benzo[d]imidazole-2-thione (1) was subjected to a Mannich reaction with either dimethylamine, urotropine, morpholine, thiomorpholine, (±) 3,3,5 trimethylhexahydroazepine, piperazine or p-bromoaniline and formalin in different molar ratios to afford the Mannich bases. The reactivity of the Mannich base 5a towards indole was also investigated. In addition the condensation of hydroxymethyl derivative 10 with morpholine, benzimidazole, p-bromoaniline, tryptamine and aminiothiazole was achieved.

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