25347-94-8 Usage
General Description
1-tert-butyl-3-methylurea is a chemical compound with the molecular formula C6H14N2O. It is a urea derivative, specifically a substituted urea, with a tert-butyl group and a methyl group attached to the nitrogen atom. 1-tert-butyl-3-methylurea is commonly used as a reagent in organic synthesis and pharmaceutical research. It is also known for its potential application as a corrosion inhibitor and a stabilizer for explosives. Additionally, 1-tert-butyl-3-methylurea has been studied for its antifungal and antiviral properties, making it a versatile and important compound in various scientific and industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 25347-94-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,3,4 and 7 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 25347-94:
(7*2)+(6*5)+(5*3)+(4*4)+(3*7)+(2*9)+(1*4)=118
118 % 10 = 8
So 25347-94-8 is a valid CAS Registry Number.
25347-94-8Relevant articles and documents
An empirical estimation of the interactions Hδ+...Cl-. The crystal and molecular structure of the 1-methyl-2-tert-butylamino-4-isopropyl-5(4H)-imidazolone hydrochloride
Krygowski,Grabowski,Anulewicz-Ostrowska,Izdebski,Fiertek
, p. 129 - 135 (2007/10/03)
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SUPPRESSION OF THE CONVERSION OF 3-t-BUTYL-1-METHYL-1-NITROSOTHIOUREA TO 3-t-BUTYL-1-METHYLUREA BY β-CYCLODEXTRIN UNDER ACIDIC CONDITIONS
Isobe, Masayoshi
, p. 65 - 68 (2007/10/02)
The denitrosation of 3-t-butyl-1-methyl-1-nitrosothiourea (1) was retarded by β-, and γ-cyclodextrins (CDs) at pH 4.70.Decomposition of 1 in the presence of β-CD produced selectively 3-t-butyl-1-methylthiourea (1a), which was remarkably different from the product ratio in the absence of β-CD.These results may be caused by both the protective and the microsolvent effect of β-CD.
THE SYNTHESIS OF ANTINEOPLASTIC AGENTS. XXXII. N-NITROSOUREAS. I.
JOHNSTON,MCCALEB,MONTGOMERY
, p. 669 - 681 (2007/10/04)
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