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3-(3-Oxo-cyclopentyl)-propionic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

34399-77-4

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34399-77-4 Usage

Synthesis Reference(s)

The Journal of Organic Chemistry, 37, p. 1947, 1972 DOI: 10.1021/jo00977a019

Check Digit Verification of cas no

The CAS Registry Mumber 34399-77-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,3,9 and 9 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 34399-77:
(7*3)+(6*4)+(5*3)+(4*9)+(3*9)+(2*7)+(1*7)=144
144 % 10 = 4
So 34399-77-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H12O3/c9-7-3-1-6(5-7)2-4-8(10)11/h6H,1-5H2,(H,10,11)

34399-77-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(3-oxocyclopentyl)propanoic acid

1.2 Other means of identification

Product number -
Other names 3-(3-oxo-cyclopentyl)-propionic 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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:34399-77-4 SDS

34399-77-4Downstream Products

34399-77-4Relevant academic research and scientific papers

Homoenolic radical derived from propionic acid: A versatile reagent for the radical version of the Michael reaction

Foubelo,Lloret,Yus

, p. 9531 - 9536 (2007/10/02)

The homoenolic radical, derived from 3-iodopropionic acid (1) by reaction with in situ generated tributyltin hydride, undergoes clean carbon-carbon forming reaction with electrophilic olefins (2) yielding functionalized acids (3).

RING CLEAVAGE AND RECONSTRUCTION OF FIVE AND SIX MEMBERED RING

Suemune, Hiroshi,Oda, Kozo,Sakai, Kiyoshi

, p. 3373 - 3376 (2007/10/02)

Under the acetalization conditions using BF3-etherate/ethylene glycol, cyclopentanones and cyclohexanones with the carbonyl function at the C3- or C4-position of the β-side chain undergo the facile ring cleavage to reconstruct the new ring.

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