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2,6-di-tert-butyl-4-[(2,5-dimethoxyphenyl)imino]cyclohexa-2,5-dien-1-one is a complex organic compound with a molecular formula of C22H31NO4. It is characterized by a cyclohexadienone core, which is a six-membered ring with alternating double bonds, and a 2,5-dien-1-one functional group, indicating a carbonyl group at the 1-position and double bonds at the 2 and 5 positions. The molecule also features two tert-butyl groups at the 2 and 6 positions, which are bulky, non-reactive alkyl groups that provide steric hindrance. Additionally, it has a 2,5-dimethoxyphenyl group attached to the imino nitrogen, which contributes to the compound's electronic properties and potential reactivity. 2,6-di-tert-butyl-4-[(2,5-dimethoxyphenyl)imino]cyclohexa-2,5-dien-1-one is known for its antioxidant properties and is used as a stabilizer in industrial applications, particularly in the polymer and rubber industries, to prevent degradation caused by heat, light, and oxygen.

5813-75-2

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5813-75-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5813-75-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,1 and 3 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5813-75:
(6*5)+(5*8)+(4*1)+(3*3)+(2*7)+(1*5)=102
102 % 10 = 2
So 5813-75-2 is a valid CAS Registry Number.

5813-75-2SDS

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 2,6-ditert-butyl-4-(2,5-dimethoxyphenyl)iminocyclohexa-2,5-dien-1-one

1.2 Other means of identification

Product number -
Other names 2,6-di-tert-butyl-4-[(2,5-dimethoxyphenyl)imino]cyclohexa-2,5-dien-1-one

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 -
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More Details:5813-75-2 SDS

5813-75-2Downstream Products

5813-75-2Relevant academic research and scientific papers

Synthesis and Characterization of (Methoxy(thiocarbonyl))sulfenyl Chloride

Schroll, Alayne L.,Eastep, Steven J.,Barany, George

, p. 1475 - 1479 (2007/10/02)

(Methoxy(thiocarbonyl))sulfenyl chloride (1), a previously elusive compound, has now been generated by cleavage of methoxy(thiocarbonyl) N-methyl-N-phenylamino sulfide (7) with gaseous hydrogen chloride.The sulfenyl chloride 1 had limited stability and was characterized by trapping with O,O'-dimethyl thiocarbonate or with methanethiol to yield (methoxycarbonyl)(methoxy(thiocarbonyl))disulfane (8) or (methoxy(thiocarbonyl))methyldisulfane (9), respectively.Chlorination of acetyl methoxy(thiocarbonyl) sulfide (6) could be arrested at 1 plus acetyl chloride, and further chlorination of 1 provided (methoxydichloromethyl)disulfanyl chloride (5).

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