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1-(2-methylbutan-2-yl)-4-nitro-benzene, also known as p-nitro-tert-butylbenzene, is an aromatic compound with the formula C10H13NO2. It is characterized by its yellow crystalline solid appearance, featuring a nitro group and a tert-butyl group attached to a benzene ring. This versatile chemical serves as a crucial intermediate in various industrial applications, including the synthesis of pharmaceuticals, agrochemicals, perfumes, food products, rubber antioxidants, and fuel additives.

6284-98-6

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6284-98-6 Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
1-(2-methylbutan-2-yl)-4-nitro-benzene is used as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its unique structure allows for the development of new compounds with potential therapeutic and pesticidal properties.
Used in Perfumery and Flavor Industry:
This aromatic compound is utilized as a fragrance and flavoring agent in the production of perfumes and food products. Its distinct scent and taste profile contribute to the creation of unique and appealing sensory experiences in these consumer goods.
Used in Rubber and Fuel Industries:
1-(2-methylbutan-2-yl)-4-nitro-benzene is employed in the synthesis of rubber antioxidants and fuel additives. Its presence in these applications helps to enhance the performance and longevity of rubber products and improve the efficiency and quality of fuels.
However, it is essential to handle 1-(2-methylbutan-2-yl)-4-nitro-benzene with caution due to its toxic nature if ingested and its potential to cause skin and eye irritation. Proper safety measures should be implemented during its production, storage, and use to minimize health risks and environmental impact.

Check Digit Verification of cas no

The CAS Registry Mumber 6284-98-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,8 and 4 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6284-98:
(6*6)+(5*2)+(4*8)+(3*4)+(2*9)+(1*8)=116
116 % 10 = 6
So 6284-98-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H15NO2/c1-4-11(2,3)9-5-7-10(8-6-9)12(13)14/h5-8H,4H2,1-3H3

6284-98-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-methylbutan-2-yl)-4-nitrobenzene

1.2 Other means of identification

Product number -
Other names p-tert-amylnitrobenzene

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:6284-98-6 SDS

6284-98-6Relevant academic research and scientific papers

BENZIIMIDAZOLE AND IMIDAZOPYRIDINE DERIVATIVES AS SODIUM CHANNEL MODULATORS

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Page/Page column 179, (2013/08/15)

The invention relates to benzimidazole and imidazopyridine derivatives, to their use in medicine, to compositions containing them, to processes for their preparation and to intermediates used in such processes. More particularly the invention relates to new Nav1.8 modulators of formula (I) or pharmaceutically acceptable salts thereof, wherein R1, R2, R3, R4, R5, R6, R7. X and Y are as defined in the description. Nav1.8 modulators are potentially useful in the treatment of a wide range of disorders, particularly pain.

The regioselectivity of internal hydrogen abstraction by triplet o-tert-amylbenzophenone

Wagner, Peter J.,Pabon, Raul,Park, Bong-Ser,Zand, Ali R.,Ward, Donald L.

, p. 589 - 596 (2007/10/02)

The title ketone undergoes triplet-state δ-hydrogen abstraction to produce two diastereomeric sets of 1-phenyl-1-indanols: the 2,3,3-trimethyl isomers 2Z and 2E by abstraction of a methylene hydrogen and the 3-methyl 3-ethyl isomers 1Z and 1E by abstracti

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