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56150-35-7

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56150-35-7 Usage

Type of compound

Synthetic flavoring agent

Origin

Derived from natural vanillin

Flavor characteristics

Stronger and more persistent than natural vanillin

Common uses

Production of chocolate, ice cream, baked goods, perfumes, and pharmaceuticals

Safety

Considered safe for consumption in small amounts

Potential side effects

Can cause skin irritation and allergic reactions in some individuals

Purpose

Enhances and intensifies the aroma and taste of various products

Check Digit Verification of cas no

The CAS Registry Mumber 56150-35-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,1,5 and 0 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 56150-35:
(7*5)+(6*6)+(5*1)+(4*5)+(3*0)+(2*3)+(1*5)=107
107 % 10 = 7
So 56150-35-7 is a valid CAS Registry Number.

56150-35-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-bis(2-phenylethyl)pyran-4-one

1.2 Other means of identification

Product number -
Other names 2,6-Diphenethyl-4H-pyran-4-one

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:56150-35-7 SDS

56150-35-7Downstream Products

56150-35-7Relevant articles and documents

Regiodivergent Hydration-Cyclization of Diynones under Gold Catalysis

Mu?oz, Miguel A.,Sanz, Roberto,Solas, Marta,Suárez-Pantiga, Samuel

supporting information, p. 7681 - 7687 (2020/10/12)

Skipped diynones, efficiently prepared from biomass-derived ethyl lactate, undergo a tandem hydration-oxacyclization reaction under gold(I) catalysis. Reaction conditions have been developed for a switchable process that allows selective access to 4-pyrones or 3(2H)-furanones from the same starting diynones. Further application of this methodology in the total synthesis of polyporapyranone B was demonstrated.

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