Welcome to LookChem.com Sign In|Join Free
  • or
2H-Pyran-2-one, 3-(benzoyloxy)tetrahydro- is a complex organic compound with the molecular formula C12H14O4. It is a derivative of 2H-pyran-2-one, featuring a benzoyloxy group attached to the tetrahydro structure. 2H-Pyran-2-one, 3-(benzoyloxy)tetrahydro- is characterized by its heterocyclic structure, with a pyran ring and a carbonyl group. It is known for its potential applications in the synthesis of various pharmaceuticals and organic compounds due to its unique chemical properties. The benzoyloxy group provides a protecting function for the hydroxyl group, which can be crucial in certain chemical reactions. 2H-Pyran-2-one, 3-(benzoyloxy)tetrahydro- is typically used as an intermediate in organic synthesis, particularly in the preparation of complex molecules that require the pyran ring system.

87532-11-4

Post Buying Request

87532-11-4 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

87532-11-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87532-11-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,5,3 and 2 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 87532-11:
(7*8)+(6*7)+(5*5)+(4*3)+(3*2)+(2*1)+(1*1)=144
144 % 10 = 4
So 87532-11-4 is a valid CAS Registry Number.

87532-11-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-oxooxan-3-yl) benzoate

1.2 Other means of identification

Product number -
Other names 2H-Pyran-2-one,3-(benzoyloxy)tetrahydro

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:87532-11-4 SDS

87532-11-4Downstream Products

87532-11-4Relevant academic research and scientific papers

Oxidation of Alkyl Trimethylsilyl Ketene Acetals with Lead(IV)

Rubottom, George M.,Gruber, John M.,Marrero, Roberto,Juve, Henrik D.,Kim, Wan Chong

, p. 4940 - 4944 (2007/10/02)

Alkyl trimethylsilyl ketene acetals generated from either esters or lactones react with lead(IV) acetate (LTA) or lead(IV) benzoate (LTB) to afford useful yields of the corresponding α-carboyloxy esters and α-carboyloxy lactones.Yields of the reaction products are optimized by use of the appropriate solvent (methylene chloride or benzene) during oxidation.Alkyl groups such as methyl, ethyl, and tert-butyl are all compatible with the procedure, and lactones containing five-, six-, and seven-membered rings give good yields of oxidation products.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 87532-11-4