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Thiourea, N-butyl-N'-(2-iodophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

53305-95-6

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53305-95-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53305-95-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,3,0 and 5 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 53305-95:
(7*5)+(6*3)+(5*3)+(4*0)+(3*5)+(2*9)+(1*5)=106
106 % 10 = 6
So 53305-95-6 is a valid CAS Registry Number.

53305-95-6SDS

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-butyl-3-(2-iodophenyl)thiourea

1.2 Other means of identification

Product number -
Other names N-n-Butyl-N'-o-iodphenylthioharnstoff

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:53305-95-6 SDS

53305-95-6Downstream Products

53305-95-6Relevant academic research and scientific papers

Metal-free synthesis of 2-substituted (N, O, C) Benzothiazoles via an intramolecular C-S bond formation

Feng, Enguang,Huang, He,Zhou, Yu,Ye, Deju,Jiang, Hualiang,Liu, Hong

experimental part, p. 422 - 429 (2010/09/05)

An efficient, economical, and convenient method was developed for the preparation of 2-substituted (N, O, C) benzothiazoles from N′-substituted- N-(2-halophenyl)thioureas, O′-substituted-N-(2-halophenyl) carbamothioates, or N-(2-halophenyl) thioamides via a base-promoted cyclization in dioxane without any transition metal. A one-pot variant combining the synthesis of the thiourea and the cyclization was also demonstrated. High yields were obtained, and a variety of functional groups were tolerated under these conditions. Transition-metal-free, mild reactive conditions, wide application scope, and shorter reaction times make this method superior to the reported methods for the synthesis of 2-substituted benzothiazoles and suitable for combinatorial format.

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