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131358-04-8

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131358-04-8 Usage

Physical state

Colorless liquid

Odor

Sweet, floral

Uses

Synthetic fragrance and flavoring agent

Found in

Perfumes, colognes, air fresheners

Industrial applications

Solvent in various processes

Role in production

Intermediate in the production of other chemicals

Stability

Relatively stable and non-reactive under normal conditions

Versatility

Widely used in the chemical industry

Safety concerns

May cause skin and eye irritation

Hazardous properties

Flammable liquid

Check Digit Verification of cas no

The CAS Registry Mumber 131358-04-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,3,5 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 131358-04:
(8*1)+(7*3)+(6*1)+(5*3)+(4*5)+(3*8)+(2*0)+(1*4)=98
98 % 10 = 8
So 131358-04-8 is a valid CAS Registry Number.

131358-04-8Downstream Products

131358-04-8Relevant articles and documents

Highly selective conversion of guaiacol to: Tert -butylphenols in supercritical ethanol over a H2WO4 catalyst

Mai, Fuhang,Cui, Kai,Wen, Zhe,Wu, Kai,Yan, Fei,Chen, Mengmeng,Chen, Hong,Li, Yongdan

, p. 2764 - 2771 (2019)

The conversion of guaiacol is examined at 300 °C in supercritical ethanol over a H2WO4 catalyst. Guaiacol is consumed completely, meanwhile, 16.7% aromatic ethers and 80.0% alkylphenols are obtained. Interestingly, tert-butylphenols are produced mainly with a high selectivity of 71.8%, and the overall selectivity of 2,6-di-tert-butylphenol and 2,6-di-tert-butyl-4-ethylphenol is as high as 63.7%. The experimental results indicate that catechol and 2-ethoxyphenol are the intermediates. Meanwhile, the WO3 sites play an important role in the conversion of guaiacol and the Br?nsted acid sites on H2WO4 enhance the conversion and favour a high selectivity of the tert-butylphenols. The recycling tests show that the carbon deposition on the catalyst surface, the dehydration and partial reduction of the catalyst itself are responsible for the decay of the H2WO4 catalyst. Finally, the possible reaction pathways proposed involve the transetherification process and the alkylation process during guaiacol conversion.

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