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15760-26-6

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15760-26-6 Usage

General Description

1-cyano-2-methylisothiourea, also known as Methylisothiourea (MITU), is a synthetic chemical compound with the molecular formula C3H6N4S. It is a potent inhibitor of nitric oxide synthase, an enzyme involved in the production of nitric oxide, a molecule that plays a key role in various physiological and pathological processes. MITU has been studied for its potential therapeutic applications in conditions such as septic shock, inflammation, and neurodegenerative diseases. However, it is important to note that MITU is also a known toxic compound, and exposure to high levels of it can pose serious health risks. Therefore, proper handling and safety precautions are essential when working with this chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 15760-26-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,7,6 and 0 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 15760-26:
(7*1)+(6*5)+(5*7)+(4*6)+(3*0)+(2*2)+(1*6)=106
106 % 10 = 6
So 15760-26-6 is a valid CAS Registry Number.

15760-26-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl N'-cyanocarbamimidothioate

1.2 Other means of identification

Product number -
Other names 3-cyano-2-methylisothiourea

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:15760-26-6 SDS

15760-26-6Relevant articles and documents

Catalyst-free synthesis of thiazolidines: Via sequential hydrolysis/rearrangement reactions of 5-arylidenethiazolidin-4-ones at room temperature

Zeng, Fanxun,Zhang, Letian,Shao, Xusheng,Li, Zhong,Xu, Xiaoyong

supporting information, p. 1932 - 1938 (2018/03/23)

A catalyst-free sequential reaction involving hydrolysis and intramolecular aza-Michael addition was developed for synthesizing functionalized thiazolidines from 5-arylidenethiazolidin-4-ones at room temperature. A series of thiazolidine-5-carboxylic acids were prepared in good to excellent yields (up to 97% yield) and excellent diastereoselectivities (up to >20:1 dr). This methodology was applicable to the construction of derivatives of thiacloprid and flutianil with good yields.

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