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2-sec-butyl-1,4-dimethylbenzene is an organic compound with the molecular formula C12H18. It is a derivative of benzene, featuring a sec-butyl group (a four-carbon alkyl chain with a branching point) at the 2-position and two methyl groups at the 1 and 4 positions. This aromatic hydrocarbon is a colorless liquid with a distinctive odor and is insoluble in water but soluble in organic solvents. It is synthesized through various chemical reactions, such as alkylation or Friedel-Crafts alkylation, and is used in the production of various chemicals, including pharmaceuticals, dyes, and fragrances. Due to its complex structure and potential environmental impact, it is important to handle and dispose of 2-sec-butyl-1,4-dimethylbenzene with care.

3561-84-0

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3561-84-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3561-84-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,6 and 1 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3561-84:
(6*3)+(5*5)+(4*6)+(3*1)+(2*8)+(1*4)=90
90 % 10 = 0
So 3561-84-0 is a valid CAS Registry Number.

3561-84-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-sec-butyl-1,4-dimethylbenzene

1.2 Other means of identification

Product number -
Other names 2-sec-Butyl-p-xylol

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:3561-84-0 SDS

3561-84-0Downstream Products

3561-84-0Relevant academic research and scientific papers

Iron oxide nanoparticles grown on carboxy-functionalized graphite: An efficient reusable catalyst for alkylation of arenes

Rajpara, Vikul,Banerjee, Subhash,Sereda, Grigoriy

experimental part, p. 2835 - 2840 (2010/10/04)

Here we report a simple procedure for the synthesis of a novel hybrid catalyst by growing iron oxide nanoparticles on carboxy-functionalized graphite. This hybrid catalyst demonstrated superior catalytic activity towards the alkylation of arenes with alkyl halides in contrast to commercial graphite or unsupported iron oxide nanoparticles in terms of yields and general applicability. The catalyst can be reused up to five times with a minimal loss of catalytic activity. Georg Thieme Verlag Stuttgart.

The synthetic potential of graphite-catalyzed alkylation

Sereda, Grigoriy A.,Rajpara, Vikul B.,Slaba, Ryan L.

, p. 8351 - 8357 (2008/02/07)

Unmodified graphite is introduced as a mild catalyst for alkylation of aromatic compounds and primary alcohols, applicable when utilization of strong Lewis acids is not feasible. The electrophilic intermediate has a significant carbocationic character and can be formed on a partially rate-limiting step.

Direct functionalization of arenes by primary alcohol sulfonate esters catalyzed by gold(III)

Shi, Zhangjie,He, Chuan

, p. 13596 - 13597 (2007/10/03)

Alkylation of arenes by primary alcohol triflate or methanesulfonate esters can be efficiently catalyzed by AuCl3 with silver triflate. Copyright

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