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13936-26-0

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13936-26-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13936-26-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,9,3 and 6 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 13936-26:
(7*1)+(6*3)+(5*9)+(4*3)+(3*6)+(2*2)+(1*6)=110
110 % 10 = 0
So 13936-26-0 is a valid CAS Registry Number.

13936-26-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-pentylbenzoyl)benzoic acid

1.2 Other means of identification

Product number -
Other names Benzoic acid,2-(4-pentylbenzoyl)

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:13936-26-0 SDS

13936-26-0Relevant articles and documents

2 - (4 -amyl benzoyl) benzoic acid and 2 -pentyl anthraquinone and preparation method thereof (by machine translation)

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Paragraph 0032-0067, (2020/11/22)

2 - (4 -pentylbenzoyl) benzoic acid and 2 -pentyl anthraquinone and a preparation method thereof relate to the technical field of fine chemicals. The preparation method of 2 - (4 -pentylbenzoyl) benzoic acid with a high tertiary-secondary ratio comprises the following steps: reacting phthalic anhydride, a solvent, a Fourier reaction catalyst and tert-amyl benzene in a hypergravity reactor, and introducing a working gas in the reaction process. ABB acid was significantly boosted after the reaction, so that the 2 -pentyraquinone obtained had a high tertiary-to-secondary ratio. The hydrogen chloride gas generated in the reaction process can be effectively removed, the isomerization reaction quantity is reduced, and the tertiary secondary ratio of the product is improved. (by machine translation)

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