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3282-56-2

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3282-56-2 Usage

Purification Methods

Recrystallise it three times by partially freezing a mixture of the mono-nitro isomers, then recrystallise it twice from MeOH and dry it in vacuo [Brown J Am Chem Soc 81 3232 1959]. [Beilstein 5 H 418, 5 I 203, 5 II 321, 5 III 943, 5 IV 1052.]

Check Digit Verification of cas no

The CAS Registry Mumber 3282-56-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,8 and 2 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3282-56:
(6*3)+(5*2)+(4*8)+(3*2)+(2*5)+(1*6)=82
82 % 10 = 2
So 3282-56-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H13NO2/c1-10(2,3)8-4-6-9(7-5-8)11(12)13/h4-7H,1-3H3

3282-56-2 Well-known Company Product Price

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  • Alfa Aesar

  • (L06067)  1-tert-Butyl-4-nitrobenzene, 98%   

  • 3282-56-2

  • 2g

  • 291.0CNY

  • Detail
  • Alfa Aesar

  • (L06067)  1-tert-Butyl-4-nitrobenzene, 98%   

  • 3282-56-2

  • 10g

  • 913.0CNY

  • Detail
  • Alfa Aesar

  • (L06067)  1-tert-Butyl-4-nitrobenzene, 98%   

  • 3282-56-2

  • 50g

  • 3268.0CNY

  • Detail

3282-56-2SDS

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 1-TERT-BUTYL-4-NITROBENZENE

1.2 Other means of identification

Product number -
Other names tert-butyl-4-nitrobenzene

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:3282-56-2 SDS

3282-56-2Relevant articles and documents

Brightly shining nanoparticles: Lipophilic perylene bisimides in aqueous phase

Langhals, Heinz

, p. 21 - 23 (2008)

The dispersion of lipophilic perylene bisimides down to nanoparticle dimensions opens the aqueous phase to these highly fluorescent, water insoluble materials. The Royal Society of Chemistry and the Centre National de la Recherche Scientifique.

NITRATION

-

Page/Page column 36; 41; 46; 64; 37, (2020/05/28)

The present invention relates to a process for preparing a nitrated compound, comprising the step of reacting a compound (A) comprising at least one substituted or unsubstituted aromatic or heteroaromatic ring, wherein said heteroaromatic ring comprises at least one heteroatom selected from the group consisting of oxygen, sulfur, phosphor, selenium and nitrogen, with a compound of formula (I) wherein Y is selected from the group consisting of hydrogen and nitro.

Nucleophilic Iron Complexes in Proton-Transfer Catalysis: An Iron-Catalyzed Dimroth Cyclocondensation

Baykal, Aslihan,Zhang, Dihan,Knelles, Jakob,Alt, Isabel T.,Plietker, Bernd

supporting information, p. 3003 - 3010 (2019/08/21)

The nucleophilic iron complex Bu4N[Fe(CO)3(NO)] (TBA[Fe]) is an active catalyst in C?H-amination but also in proton-transfer catalysis. Herein, we describe the successful use of this complex as a proton-transfer catalyst in the cyclocondensation reaction between azides and ketones to the corresponding 1,2,3-triazoles. Cross-experiments indicate that the proton-transfer catalysis is significantly faster than the nitrene-transfer catalysis, which would lead to the C?H amination product. An example of a successful sequential Dimroth triazole–indoline synthesis to the corresponding triazole-substituted indolines is presented.

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