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1704-16-1

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1704-16-1 Usage

General Description

2,4-Pentanedione, 3-(1-hydroxyethylidene)- is a chemical compound with the molecular formula C7H12O3. It is a diketone with a hydroxyethylidene group attached to the third carbon atom. 2,4-Pentanedione, 3-(1-hydroxyethylidene)- is commonly used as a flavoring agent in food and beverages due to its buttery and creamy flavor profile. It is also used in the production of fragrances and as a chemical intermediate in the synthesis of other organic compounds. However,

Check Digit Verification of cas no

The CAS Registry Mumber 1704-16-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,0 and 4 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1704-16:
(6*1)+(5*7)+(4*0)+(3*4)+(2*1)+(1*6)=61
61 % 10 = 1
So 1704-16-1 is a valid CAS Registry Number.

1704-16-1SDS

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 triacetylmethane

1.2 Other means of identification

Product number -
Other names 3-acetyl-pentane-2,4-dione enol tautomer

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:1704-16-1 SDS

1704-16-1Upstream product

1704-16-1Relevant articles and documents

Unusual aluminum chloride-assisted conversion of isopropenyl acetate into 3-acetyl- and 3,5-diacetyl-2,6-dimethyl-4H-pyran-4-ones

Novikov,Shestak,Denisenko

experimental part, p. 1600 - 1604 (2011/05/04)

Reflux of isopropenyl acetate with an excess of AlCl3 in 1,2-dichloroethane affords 3,5-diacetyl-2,6-dimethyl-4H-pyran-4-one in 17% yield. The mild acidic cleavage of the latter (2% HCl, 20°C, 16 h) gives 3-acetyl-2,6-dimethyl-4H-pyran-4-one in 87% yield, whereas this reaction under more drastic conditions (17% HCl, reflux, 3 h) gives 2,6-dimethyl-4H-pyran-4-one in 61% yield.

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