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2H-Pyran-3(6H)-one, 4-(benzoyloxy)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75414-40-3

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75414-40-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75414-40-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,4,1 and 4 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 75414-40:
(7*7)+(6*5)+(5*4)+(4*1)+(3*4)+(2*4)+(1*0)=123
123 % 10 = 3
So 75414-40-3 is a valid CAS Registry Number.

75414-40-3SDS

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 (5-oxo-2H-pyran-4-yl) benzoate

1.2 Other means of identification

Product number -
Other names -

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:75414-40-3 SDS

75414-40-3Downstream Products

75414-40-3Relevant academic research and scientific papers

A convenient access to the 1,5-anhydro forms of d-tagatose, l-rhamnulose and d-xylulose via 2-hydroxyglycal esters

Jarglis, Pan,Goeckel, Volker,Lichtenthaler, Frieder W.

experimental part, p. 952 - 960 (2009/10/10)

Zemplen methanolysis or a three-step protocol comprising hydroxylaminolysis, de-O-acetylation and deoximination smoothly and efficiently convert the benzoylated 2-hydroxy-d-glycals of d-galactose, l-rhamnose and d-xylose into their configurationally relat

A CONVENIENT ACCESS TO 1,5-ANHYDROKETOSES

Lichtenthaler, F. W.,Ashry E. S. H. El,Goeckel, V. H.

, p. 1429 - 1432 (2007/10/02)

A convenient, verstile entry into the 1,5-anhydroketose series is described and their conversion into enolones, enolone oximes and γ-pyrones.

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