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5180-48-3

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5180-48-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5180-48-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,8 and 0 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5180-48:
(6*5)+(5*1)+(4*8)+(3*0)+(2*4)+(1*8)=83
83 % 10 = 3
So 5180-48-3 is a valid CAS Registry Number.

5180-48-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name acetic acid,2,4,6-tritert-butylphenol

1.2 Other means of identification

Product number -
Other names Phenol,2,4,6-tris(1,1-dimethylethyl)-,acetate

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:5180-48-3 SDS

5180-48-3Downstream Products

5180-48-3Relevant articles and documents

Silica gel-supported phosphotungstic acid (PTA) catalysed acylation of alcohols and phenols with acetic anhydride under mild reaction conditionst

Jin, Tong-Shou,Xiao, Jin-Chong,Wang, Zhen-Hua,Li, Tong-Shuang

, p. 412 - 414 (2007/10/03)

Phosphotungstic acid, which is commercially available, practically and efficiently catalyses the acylation of a series of alcohols and phenols with acetic anhydride at room temperature of at refluxing temperature.

SYNTHESIS OF 4-ALKOXY- AND 4-ACYLOXY-2,6-DI-tert-BUTYLPHENOLS AND QUINOL ETHERS BASED ON THEM

Dobronravova, Z. A.,Meshcheryakov, V. I.,Prishchenko, Yu. E.,Gavrilov, L. D.,Vereshchagin, L. I.

, p. 910 - 914 (2007/10/02)

4-Alkoxy- and 4-acyloxy-2,6-di-tert-butylphenols were obtained by the alkylation and acylation of 2,6-di-tert-butyl-p-dihydroxybenzene.With quinone dioximes under oxidizing conditions the products form quinol ethers.

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