Welcome to LookChem.com Sign In|Join Free

CAS

  • or

6279-89-6

4-tert-butyl-2,6-dimethylnitrobenzene is an organic compound with the chemical formula C??H??NO?. It is a derivative of nitrobenzene, characterized by the presence of a nitro group (-NO?) attached to a benzene ring. The molecule also features a tert-butyl group (-C(CH?)?) at the 4-position and two methyl groups (-CH?) at the 2 and 6 positions. 4-TERT-BUTYL-2,6-DIMETHYLNITROBENZENE is known for its potential applications in the synthesis of various chemicals and materials, such as dyes, pharmaceuticals, and polymers. Due to its reactivity and the presence of functional groups, it is often used as an intermediate in chemical reactions. However, it is important to handle 4-TERT-BUTYL-2,6-DIMETHYLNITROBENZENE with care, as it may pose health and environmental risks due to its nitroaromatic nature.

6279-89-6 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 6279-89-6 Structure

  • Basic information

    1. Product Name: 4-TERT-BUTYL-2,6-DIMETHYLNITROBENZENE
    2. Synonyms: 4-TERT-BUTYL-2,6-DIMETHYLNITROBENZENE;5-(tert-butyl)-1,3-dimethyl-2-nitrobenzene;5-TERT-BUTYL-2-NITRO-M-XYLENE
    3. CAS NO:6279-89-6
    4. Molecular Formula: C12H17NO2
    5. Molecular Weight: 207.27
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 6279-89-6.mol

  • Chemical Properties

    1. Melting Point: 84-85 °C
    2. Boiling Point: 279.1°C at 760 mmHg
    3. Flash Point: 106.5°C
    4. Appearance: /
    5. Density: 1.033g/cm3
    6. Vapor Pressure: 0.00696mmHg at 25°C
    7. Refractive Index: 1.518
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 4-TERT-BUTYL-2,6-DIMETHYLNITROBENZENE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 4-TERT-BUTYL-2,6-DIMETHYLNITROBENZENE(6279-89-6)
    12. EPA Substance Registry System: 4-TERT-BUTYL-2,6-DIMETHYLNITROBENZENE(6279-89-6)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 6279-89-6(Hazardous Substances Data)

6279-89-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6279-89-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,7 and 9 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6279-89:
(6*6)+(5*2)+(4*7)+(3*9)+(2*8)+(1*9)=126
126 % 10 = 6
So 6279-89-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H17NO2/c1-8-6-10(12(3,4)5)7-9(2)11(8)13(14)15/h6-7H,1-5H3

6279-89-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-tert-butyl-1,3-dimethyl-2-nitrobenzene

1.2 Other means of identification

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

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:6279-89-6 SDS

6279-89-6Relevant articles and documents

An electroluminescent compound and an electroluminescent device comprising the same

-

Paragraph 0291-0295, (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

SUBSTITUTED NITROBENZENE DERIVATIVES AS MEDICINES AND OTHER USEFUL USES THEREOF

-

, (2008/06/13)

The present invention relates to a use of substituted nitrobenzene derivatives of general Formula I in medicine and health food, the pharmaceutical compositions comprising substituted nitrobenzene derivatives of general Formula I and the methods thereof for the prophylaxis and treatment of diseases.

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).

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 6279-89-6