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3-(2-oxotetrahydro-3-furanyl)propanoic acid, also known as saltdata free, is a chemical compound with the molecular formula C8H12O5. It is a derivative of tetrahydrofuran and propanoic acid, featuring a furan ring and a carboxylic acid group. This organic compound is characterized by its unique structure, which includes a tetrahydrofuran ring fused to a propanoic acid chain. It is used in various chemical and pharmaceutical applications, such as the synthesis of certain drugs and other bioactive molecules. The compound's properties, such as its reactivity and solubility, make it a valuable intermediate in organic synthesis.

936-83-4

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936-83-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 936-83-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,3 and 6 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 936-83:
(5*9)+(4*3)+(3*6)+(2*8)+(1*3)=94
94 % 10 = 4
So 936-83-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H10O4/c8-6(9)2-1-5-3-4-11-7(5)10/h5H,1-4H2,(H,8,9)

936-83-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(2-oxooxolan-3-yl)propanoic acid

1.2 Other means of identification

Product number -
Other names Tetrahydro-2-oxo-3-furanpropanoic acid

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

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More Details:936-83-4 SDS

936-83-4Downstream Products

936-83-4Relevant academic research and scientific papers

CONJUGATE ADDITION OF IMIDAZOLINES:A PROTOCOL FOR 1,4-ADDITION TO ENONES AND OTHER ACCEPTORS

Jones, Raymond C. F.,Hirst, Simon C.

, p. 5361 - 5364 (2007/10/02)

The enaminoester 1-benzyl-2-ethoxycarbonylmethyleneimidazolidine reacts with α,β-enones and other Michael acceptors to give 1,4-adducts; removal of the ethoxycarbonyl group completes overall conjugate addition of the imidazoline α-anion (which itself adds 1,2 to enones),and hydrolysis affords carboxylic acids.

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