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1756-31-6

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1756-31-6 Usage

General Description

1-(3,5-di-tert-butylphenyl)ethanone is a chemical compound with the molecular formula C16H22O. It is a pale yellow liquid that is commonly used as a flavoring agent in food and beverages. 1-(3,5-di-tert-butylphenyl)ethanone is also used in the production of perfumes and fragrances due to its pleasant aroma. Additionally, it has applications in the pharmaceutical and cosmetic industries. 1-(3,5-di-tert-butylphenyl)ethanone is known for its strong and long-lasting scent, making it a popular choice for adding fragrance to a variety of products. It is important to handle this chemical with care, as it can be harmful if ingested or inhaled, and can cause irritation to the skin and eyes.

Check Digit Verification of cas no

The CAS Registry Mumber 1756-31-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,5 and 6 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1756-31:
(6*1)+(5*7)+(4*5)+(3*6)+(2*3)+(1*1)=86
86 % 10 = 6
So 1756-31-6 is a valid CAS Registry Number.

1756-31-6SDS

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 1-(3,5-ditert-butylphenyl)ethanone

1.2 Other means of identification

Product number -
Other names 3,5-di-t-butylacetophenone

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:1756-31-6 SDS

1756-31-6Downstream Products

1756-31-6Relevant articles and documents

Chemical Consequences of the Mechanical Bond: A Tandem Active Template-Rearrangement Reaction

Modicom, Florian,Jamieson, Ellen M. G.,Rochette, Elise,Goldup, Stephen M.

supporting information, p. 3875 - 3879 (2019/02/24)

We report the unexpected discovery of a tandem active template CuAAC-rearrangement process, in which N2 is extruded on the way to the 1,2,3-triazole product to give instead acrylamide rotaxanes. Mechanistic investigations suggest this process i

Tropylium Ion Catalyzes Hydration Reactions of Alkynes

Oss, Giulia,Ho, Junming,Nguyen, Thanh Vinh

supporting information, p. 3974 - 3981 (2018/08/17)

The hydration of alkynes is one of the most atom-economic and versatile synthetic protocols to access carbonyl compounds. This fundamental reaction, however, often requires transition-metal catalysts or harsh reaction conditions to promote the addition of water to the carbon–carbon triple bond. In this work, it is demonstrated that the non-benzenoid aromatic tropylium ion can be used as an organic Lewis acid promoter for the hydration of alkynes under simple reaction conditions with excellent outcomes.

Design, synthesis and biological evaluation of nuclear receptor-degradation inducers

Itoh, Yukihiro,Kitaguchi, Risa,Ishikawa, Minoru,Naito, Mikihiko,Hashimoto, Yuichi

experimental part, p. 6768 - 6778 (2012/01/13)

Compounds that regulate the function(s) of nuclear receptors (NRs) are useful for biological studies and as candidate therapeutic agents. Most such compounds are agonists or antagonists. On the other hand, we have developed specific protein degradation in

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