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5082-72-4

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5082-72-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5082-72-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,8 and 2 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5082-72:
(6*5)+(5*0)+(4*8)+(3*2)+(2*7)+(1*2)=84
84 % 10 = 4
So 5082-72-4 is a valid CAS Registry Number.

5082-72-4SDS

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 4-(3,5-ditert-butyl-4-hydroxyphenyl)butan-2-one

1.2 Other means of identification

Product number -
Other names -

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:5082-72-4 SDS

5082-72-4Relevant articles and documents

Manganese-catalyzed dehydrogenative Csp3-Csp2coupling of imidazo[1,2-a]pyridines with methyl ketones

Yao, Hua,Zhong, Xiaoyang,Wang, Bingqing,Lin, Sen,Liu, Lichi,Yan, Zhaohua

, p. 3479 - 3483 (2021)

A Mn(ii)-catalyzed efficient C-H alkylation of imidazoheterocycles with methyl ketones has been developedviadehydrogenative C(sp3)-C(sp2) coupling which can serve as a novel approach toward hydrocarboxylated imidazolopyridines. The merit of this strategy is illustrated by excellent functional group tolerance and the use of cheap and readily available starting materials.

Synthesis and characterization of novel phenolic derivatives with the glycerol ketal group as an efficient antioxidant for gasoline stabilization

Namazifar, Zeinab,Saadati, Fariba,Miranbeigi, Ali Akbar

, p. 10038 - 10044 (2019/07/04)

The development of antioxidants with phenol, hydroxyl, and ketal functional groups provides a creative approach to preventing the degradation of stored petroleum-derived products such as gasoline. The present study proposes a simple and efficient protocol

AMBERLYST-15 CATALYZED ADDITION OF PHENOLS TO α,β-UNSATURATED KETONES

Bunce, Richard A.,Reeves, Henry D.

, p. 1109 - 1118 (2007/10/02)

Amberlyst-15 has been used to catalyze regioselective additions of phenols to α,β-unsaturated ketones in yields of 20-90percent.The reaction is superior to the analogous reaction employing concentrated sulfuric acid in affording greater yields and purer products with a minimum of laboratory operations.

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