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2,5-Heptanedione, 6,6-dimethyl-3-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

112481-16-0

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112481-16-0 Usage

Physical form

Yellow to brown solid

Odor

Strong

Uses

Flavoring ingredient in food industry, fragrance in cosmetic industry, synthesis of pharmaceuticals and agrochemicals

Chemical classification

Ketone

Flammability

Flammable, potential fire hazard

Health hazards

Skin, eye, and respiratory system irritation; caution advised in handling and industrial use

Check Digit Verification of cas no

The CAS Registry Mumber 112481-16-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,4,8 and 1 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 112481-16:
(8*1)+(7*1)+(6*2)+(5*4)+(4*8)+(3*1)+(2*1)+(1*6)=90
90 % 10 = 0
So 112481-16-0 is a valid CAS Registry Number.

112481-16-0SDS

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 6,6-dimethyl-3-phenylheptane-2,5-dione

1.2 Other means of identification

Product number -
Other names 2,5-Heptanedione,6,6-dimethyl-3-phenyl

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:112481-16-0 SDS

112481-16-0Downstream Products

112481-16-0Relevant academic research and scientific papers

Nucleophilic Addition to Tricarbonyliron Complexes of α,β-Unsaturated Ketones and the Production of 1,4-Diketones

Danks, Timothy N.,Rakshit, Devajyoti,Thomas, Susan E.

, p. 2091 - 2094 (2007/10/02)

The first examples of nucleophilic addition to tricarbonyliron complexes α,β-unsaturated ketones are described.Addition of Grignard, organolithium, and organocuprate reagents to the tricarbonyliron complex of benzylideneacetone (1) gives 1,4-diketones.The synthesis and reactivity of the tricarbonyliron complexes of PhCH=CHCOR, R=Bu (7), R=Bui (8), and R=But (9) are reported.

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