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5-Hydroxy-2,2-dimethyltetrahydrofuran-3-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

35298-49-8

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35298-49-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35298-49-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,2,9 and 8 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 35298-49:
(7*3)+(6*5)+(5*2)+(4*9)+(3*8)+(2*4)+(1*9)=138
138 % 10 = 8
So 35298-49-8 is a valid CAS Registry Number.

35298-49-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-hydroxy-2,2-dimethyloxolan-3-one

1.2 Other means of identification

Product number -
Other names 5-Hydroxy-2,2-dimethyltetrahydrofuran-3-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:35298-49-8 SDS

35298-49-8Relevant academic research and scientific papers

Pheromone synthesis. Part 264: Synthesis of the core 3-oxabicyclo[3.3.0]octane structures of gomadalactones A, B and C, the components of the contact sex pheromone of the white-spotted longicorn beetle, Anoplophora malasiaca

Mori, Kenji

, p. 3387 - 3398 (2019/05/15)

The core bicyclic cyclopentanelactone structures of gomadalactones A, B and C with α-hydroxyketone system were synthesized from (R)-pulegone, employing deconjugation of an α,β-unsaturated lactone as the key step. Comparison of the CD spectra of the synthetic compounds with those of the natural products confirmed the absolute configuration of the natural pheromone components as proposed in 2007. X-ray crystallographic analysis of the model compound of gomadalactone B core structure was carried out.

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