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5-tert-butyl-1,3-benzodioxole is an organic compound characterized by a benzene ring with a dioxole (oxygen-containing heterocycle) fused to it, and a tert-butyl group attached to the 5th position. This molecule is known for its stability and unique electronic properties, which can influence its reactivity and applications. It is often used as a building block in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals due to its ability to modify the physical and chemical properties of these compounds. The tert-butyl group provides steric hindrance and can affect the molecule's lipophilicity, while the benzodioxole ring contributes to its aromaticity and potential for electron delocalization.

7228-36-6

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7228-36-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7228-36-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,2 and 8 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7228-36:
(6*7)+(5*2)+(4*2)+(3*8)+(2*3)+(1*6)=96
96 % 10 = 6
So 7228-36-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H9N/c11-10-6-8-4-2-1-3-5-9(8)7-10/h1-7H,11H2

7228-36-6SDS

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-benzodioxole

1.2 Other means of identification

Product number -
Other names 4-tert-butyl-1,2-(methylenedioxy)benzene

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:7228-36-6 SDS

7228-36-6Downstream Products

7228-36-6Relevant academic research and scientific papers

Nickel-catalyzed Kumada cross-coupling reactions of tertiary alkylmagnesium halides and aryl bromides/triflates

Joshi-Pangu, Amruta,Wang, Chao-Yuan,Biscoe, Mark R.

supporting information; experimental part, p. 8478 - 8481 (2011/06/25)

We report a Ni-catalyzed process for the cross-coupling of tertiary alkyl nucleophiles and aryl bromides. This process is extremely general for a wide range of electrophiles and generally occurs with a ratio of retention to isomerization >30:1. The same procedure also accommodates the use of aryl triflates, vinyl chlorides, and vinyl bromides as the electrophilic component.

FUSED AMINO PYRIDINE AS HSP90 INHIBITORS

-

Page/Page column 56, (2008/12/08)

The present invention relates to HSP90 inhibitors containing fused amino pyridine core that are useful as inhibitors of HSP90 and their use in the treatment of HSP90 related diseases and disorders such as cancer, an autoimmune disease, or a neurodegenerative disease.

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