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4-[2-oxo-2-(2-oxocyclohexyl)ethyl]piperidine-2,6-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

6276-34-2

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6276-34-2 Usage

Properties

Pale yellow crystalline solid, insoluble in water, soluble in organic solvents

Use

Photoinitiator in dental resins and adhesives

Function

Initiates photopolymerization when exposed to light, leading to polymer network formation

Concerns

Potential cytotoxicity and allergenicity

Regulation

Use in dental products regulated in some countries

Check Digit Verification of cas no

The CAS Registry Mumber 6276-34-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,7 and 6 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6276-34:
(6*6)+(5*2)+(4*7)+(3*6)+(2*3)+(1*4)=102
102 % 10 = 2
So 6276-34-2 is a valid CAS Registry Number.

6276-34-2SDS

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 4-[2-oxo-2-(2-oxocyclohexyl)ethyl]piperidine-2,6-dione

1.2 Other means of identification

Product number -
Other names 2-(2,6-dioxopiperidin-4-ylacetyl)cyclohexanone

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:6276-34-2 SDS

6276-34-2Relevant academic research and scientific papers

Synthesis of dehydro derivatives of cycloheximide and inactone

Buravskaya,Lakhvich

, p. 724 - 728 (2007/10/03)

Catalytic hydrogenation of 3-chloro-2-(2,6-dioxopiperidin-4-ylacetyl)-2-cyclohexenones over palladium catalyst leads to formation of dehydrocycloheximide derivatives. Reduction of the same compounds with Zn-Ag yields dehydroinactone derivatives.

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