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4-(TERT-BUTYL)-2,6-DIMETHYLANILINE, with the molecular formula C13H21N, is an aromatic amine derivative of aniline. It features a tert-butyl group and two methyl groups attached to the nitrogen atom, giving it a pale yellow liquid appearance. 4-(TERT-BUTYL)-2,6-DIMETHYLANILINE is insoluble in water but readily soluble in organic solvents, making it a versatile and valuable chemical for various industrial applications. However, due to its potential harmful effects if ingested, inhaled, or in contact with skin, it requires careful handling.

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  • 42014-60-8 Structure
  • Basic information

    1. Product Name: 4-(TERT-BUTYL)-2,6-DIMETHYLANILINE
    2. Synonyms: 4-(TERT-BUTYL)-2,6-DIMETHYLANILINE;2-Amino-5-(tert-butyl)-m-xylene, 4-(tert-Butyl)-2,6-xylidine
    3. CAS NO:42014-60-8
    4. Molecular Formula: C12H19N
    5. Molecular Weight: 177.29
    6. EINECS: N/A
    7. Product Categories: Amines;Phenyls & Phenyl-Het;Phenyls & Phenyl-Het
    8. Mol File: 42014-60-8.mol
  • Chemical Properties

    1. Melting Point: 29-29.5 °C
    2. Boiling Point: 96 °C
    3. Flash Point: 111.8 °C
    4. Appearance: /
    5. Density: 0.928 g/cm3
    6. Vapor Pressure: 0.0102mmHg at 25°C
    7. Refractive Index: 1.525
    8. Storage Temp.: Keep in dark place,Sealed in dry,Room Temperature
    9. Solubility: N/A
    10. PKA: 4.63±0.10(Predicted)
    11. CAS DataBase Reference: 4-(TERT-BUTYL)-2,6-DIMETHYLANILINE(CAS DataBase Reference)
    12. NIST Chemistry Reference: 4-(TERT-BUTYL)-2,6-DIMETHYLANILINE(42014-60-8)
    13. EPA Substance Registry System: 4-(TERT-BUTYL)-2,6-DIMETHYLANILINE(42014-60-8)
  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: 20/21/22-36/37/38-36
    3. Safety Statements: 26-36/37/39
    4. RIDADR: 2810
    5. WGK Germany:
    6. RTECS:
    7. HazardClass: 6.1
    8. PackingGroup:
    9. Hazardous Substances Data: 42014-60-8(Hazardous Substances Data)

42014-60-8 Usage

Uses

Used in Chemical Synthesis Industry:
4-(TERT-BUTYL)-2,6-DIMETHYLANILINE is used as an intermediate in the synthesis of dyes, pigments, and pharmaceuticals for its ability to contribute to the formation of complex organic molecules that impart color and therapeutic properties.
Used in Pharmaceutical Industry:
4-(TERT-BUTYL)-2,6-DIMETHYLANILINE is used as a building block in the development of pharmaceutical compounds, leveraging its chemical structure to create new drugs with potential therapeutic benefits.
Used in Dye and Pigment Industry:
4-(TERT-BUTYL)-2,6-DIMETHYLANILINE is used as a precursor in the production of dyes and pigments, where its chemical properties allow for the creation of stable and vibrant colorants for various applications.

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

42014-60-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(tert-Butyl)-2,6-dimethylaniline

1.2 Other means of identification

Product number -
Other names 4-tert-butyl-2,6-dimethylaniline

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:42014-60-8 SDS

42014-60-8Relevant articles and documents

C-H borylation by platinum catalysis

Furukawa, Takayuki,Tobisu, Mamoru,Chatani, Naoto

, p. 332 - 342 (2017/05/09)

Herein, we describe the platinum-catalyzed borylation of aromatic C-H bonds. N-Heterocyclic carbene-ligated platinum catalysts are found to be efficient catalysts for the borylation of aromatic C(sp2)-H bonds when bis(pinacolato)diboron is used as the boron source. The most remarkable feature of these Pt catalysts is their lack of sensitivity towards the degree of steric hindrance around the C-H bonds undergoing the borylation reaction. These Pt catalysts allow for the synthesis of sterically congested 2,6-disubstituted phenylboronic esters, which are otherwise difficult to synthesize using existing C-H borylation methods. Furthermore, platinum catalysis allows for the site-selective borylation of the C-H bonds ortho to fluorine substituents in fluoroarene systems. Preliminary mechanistic studies and work towards the synthetic application of this platinum catalyzed C-H borylation process are described.

An electroluminescent compound and an electroluminescent device comprising the same

-

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

C-H Functionalization at Sterically Congested Positions by the Platinum-Catalyzed Borylation of Arenes

Furukawa, Takayuki,Tobisu, Mamoru,Chatani, Naoto

supporting information, p. 12211 - 12214 (2015/10/12)

Despite significant progress in the area of C-H bond functionalization of arenes, no general method has been reported for the functionalization of C-H bonds at the sterically encumbered positions of simple arenes, such as mesitylene. Herein, we report the development of the first platinum-based catalyst for C-H borylation of arenes and heteroarenes. Notably, this method exhibited high tolerance toward steric hindrance and provided rapid access to a series of 2,6-disubstituted phenylboronic esters, valuable building blocks for further elaborations.

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

Tellurium mediated reduction of aromatic nitro groups

Khan, Rabat H.

, p. 290 - 291 (2007/10/03)

Treatment of a wide range of aromatic nitro compounds with tellurium powder in aqueous methanolic ammonium chloride results in selective reduction of the nitro groups; ester, nitrile, amide and halide substituents are unaffected.

Metacyclophanes and Related Compounds. Part 16. Preparation of 8-Fluoro-t-butylmetacyclophanes and their Treatment with Aluminium Chloride-Nitromethane in Benzene

Yamato, Takehiko,Arimura, Takashi,Tashiro, Masashi

, p. 1 - 8 (2007/10/02)

The preparation of 8-fluoro-t-butylmetacyclophanes (5) are described.Dithiametacyclophane (3) and metacyclophane bis(sulphones) (4) were obtained as a mixture of transoid and cisoid conformers, but metacyclophanes (5) were exclusively obtained as the transoid conformer after pyrolysis of the sulphones (4).AlCl3-MeNO2-Catalyzed trans-t-butylation of 8-fluoro-16-methyl-5,13-di-t-butylmetacyclophane (5a) in benzene under a variety of conditions faild to give 8-fluoro-16-methylmetacyclophane (32) but, instead, the tetrahydropyrenes (33) and/or (34) were obtained depending upon the conditions used.Internally substituted metacyclophanes were isomerized to the strainless metacyclophanes and these were then oxidized to the tetrahydropyrene (33).

REDUCTION OF AROMATIC NITRO COMPOUNDS WITH SODIUM TELLURIDE

Suzuki, Hitomi,Manabe, Hajime,Inouye, Masahiko

, p. 1671 - 1674 (2007/10/02)

Sodium telluride, prepared by heating tellurium with Rongalite in aqueous sodium hydroxide, easily reduces aromatic nitro compounds to the corresponding amines in good yields.The reduction can be carried out using a catalytic amount of tellurium, since sodium telluride is readily regenerated in the presence of excess Rongalite.

REDUCTION OF AROMATIC AND ALIPHATIC NITRO COMPOUNDS BY SODIUM HYDROGEN TELLURIDE

Osuka, Atsuhiro,Shimizu, Hirohito,Suzuki, Hitomi

, p. 1373 - 1374 (2007/10/02)

Various nitro compounds were effectively reduced by sodium hydrogen telluride in good yields.Thus, reductive conversion of unhindered nitrobenzenes to azoxybenzenes, sterically hindered nitrobenzenes to anilines, nitroalkanes to dimer of nitrosoalkanes, and vicinal-dinitroalkane to olefin was achieved.

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