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5344-89-8

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5344-89-8 Usage

General Description

1-(2,3-dimethylbutan-2-yl)urea, also known as N-(1,1-dimethylethyl)-N'-methylurea, is a chemical compound with the molecular formula C7H16N2O. It is an organic compound classified as a urea derivative, with a tertiary butyl group attached to the nitrogen atom. 1-(2,3-dimethylbutan-2-yl)urea is commonly used as a reactant in organic synthesis and pharmaceuticals, as well as in the manufacturing of agricultural chemicals. It has a wide range of applications, including as a stabilizer in plastics and rubber, a corrosion inhibitor in lubricants, and as a reagent in chemical reactions. 1-(2,3-dimethylbutan-2-yl)urea is a white crystalline solid that is moderately soluble in water and has a relatively low melting point, making it versatile in various industrial processes.

Check Digit Verification of cas no

The CAS Registry Mumber 5344-89-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,4 and 4 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5344-89:
(6*5)+(5*3)+(4*4)+(3*4)+(2*8)+(1*9)=98
98 % 10 = 8
So 5344-89-8 is a valid CAS Registry Number.

5344-89-8SDS

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 2,3-dimethylbutan-2-ylurea

1.2 Other means of identification

Product number -
Other names 2,3-dimethyl-2-buturea

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:5344-89-8 SDS

5344-89-8Relevant articles and documents

Metal-free conversion of methane and cycloalkanes to amines and amides by employing a borylnitrene

Bettinger, Holger F.,Filthaus, Matthias,Bornemann, Holger,Oppel, Iris M.

supporting information; body text, p. 4744 - 4747 (2009/02/06)

(Chemical Equation Presented) C-H insertion: Borylnitrenes, which are generated in situ by photoylsis of azides, convert unactivated alkanes by intermolecular C-H insertion into aminoboranes (see scheme), which in turn can be reacted further to give amines or amides. The boryl group serves two purposes: it converts the nitrene into a highly reactive BN vinylidene analogue, and it is easily cleaved from the product.

Synthesis of 2H- and 3H-labelled iptakalim hydrochloride

Zhang, Cheng,Yang, Rifang,Chen, Lanfu,Zhong, Bohua,Yun, Liuhong,Wang, Hai

, p. 583 - 590 (2007/10/03)

Iptakalim hydrochloride (N-(1-methylethyl)-1,1,2-trimethyl-propylamine hydrochloride) is a promising antihypertensive drug discovered and developed by Beijing Institute of Pharmacology and Toxicology. Deuterium- and tritium-labelled compounds were designed and synthesized for pharmacokinetic and pharmacological mechanism studies. A derivatization method has been employed in the synthesis procedure. Copyright

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