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28056-54-4

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28056-54-4 Usage

General Description

2,2,4-Trimethylcyclopentanone is a chemical compound with the formula C9H16O. It is a clear, colorless liquid with a pleasant odor. This chemical is commonly used as a solvent and as a fragrance ingredient in various industrial and consumer products. It is also used in the production of flavors and fragrances due to its unique odor profile. Additionally, 2,2,4-Trimethylcyclopentanone has been investigated for its potential applications in pharmaceutical and agricultural products. Overall, this compound has a wide range of uses and applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 28056-54-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,0,5 and 6 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 28056-54:
(7*2)+(6*8)+(5*0)+(4*5)+(3*6)+(2*5)+(1*4)=114
114 % 10 = 4
So 28056-54-4 is a valid CAS Registry Number.

28056-54-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,4-trimethylcyclopentan-1-one

1.2 Other means of identification

Product number -
Other names 2,2,4-Trimethyl-cyclopentanon

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:28056-54-4 SDS

28056-54-4Relevant articles and documents

Alternative synthesis of 2-hydroxy-3,5,5-trimethylcyclopent-2-en-1-one

Chapuis, Christian,Saint-Leger, Christine

scheme or table, p. 111 - 117 (2010/04/01)

The 2-hydroxy-3,5,5-trimethylcyclopent-2-en-1-one (1) was synthesized in 42% yield by rearrangement of epoxy ketone 10 on treatment with BF3 ? Et2O under anhydrous conditions. Intermediate 10 was available from the known enone 8, either via direct epoxidation (60% H2O 2 , NaOH, MeOH; yield 50%), or via reduction to the corresponding allylic alcohol 14 (LiAlH4, THF), followed by epoxidation ([VO(acac)2], tBuOOH) and reoxidation under Swern conditions, in 37% total yield.

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