42014-60-8 Usage
General Description
4-(tert-butyl)-2,6-dimethylaniline is a chemical compound with the molecular formula C13H21N. It is an aromatic amine that is commonly used as an intermediate in the synthesis of dyes, pigments, and pharmaceuticals. 4-(TERT-BUTYL)-2,6-DIMETHYLANILINE is a derivative of aniline, containing a tert-butyl group and two methyl groups attached to the nitrogen atom. 4-(tert-butyl)-2,6-dimethylaniline is a pale yellow liquid that is insoluble in water but soluble in organic solvents. It is a versatile and valuable chemical that has a wide range of industrial applications. However, it should be handled with care as it can be harmful if ingested, inhaled, or in contact with skin.
Check Digit Verification of cas no
The CAS Registry Mumber 42014-60-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,0,1 and 4 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 42014-60:
(7*4)+(6*2)+(5*0)+(4*1)+(3*4)+(2*6)+(1*0)=68
68 % 10 = 8
So 42014-60-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H19N/c1-8-6-10(12(3,4)5)7-9(2)11(8)13/h6-7H,13H2,1-5H3
42014-60-8Relevant articles and documents
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Akamatsu et al.
, p. 1067,1070 (1961)
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An electroluminescent compound and an electroluminescent device comprising the same
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Paragraph 0291; 0296-0299, (2016/10/08)
The present invention relates to an organic light emitting compound represented by chemical formula 1, and an organic electroluminescent device comprising the same. The organic light emitting compound according to the present invention increases PL quantu
Oligomerization of ethylene using new tridentate iron catalysts bearing α-diimine ligands with pendant S and P donors
Small, Brooke L.,Rios, Ray,Fernandez, Eric R.,Gerlach, Deidra L.,Halfen, Jason A.,Carney, Michael J.
experimental part, p. 6723 - 6731 (2011/03/17)
Stoichiometric Schiff base condensations of sterically bulky primary amines with acenaphthenequinone yield isolable monoimines. In the presence of iron(II) chloride, the remaining ketone reacts with a second primary amine bearing a pendant donor atom to g
