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1,4-Dioxaspiro[4.4]nonane-6-carboxaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

66522-88-1

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66522-88-1 Usage

Chemical class

Aldehyde

Molecular structure

Spiro-cyclic ring system

Applications

a. Organic synthesis
b. Pharmaceutical production
c. Agrochemical production
d. Fine chemical production
e. Perfume and fragrance industry

Importance

Plays a significant role in the creation of valuable products

Safety precautions

Necessary due to potential health hazards if not properly managed

Check Digit Verification of cas no

The CAS Registry Mumber 66522-88-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,5,2 and 2 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 66522-88:
(7*6)+(6*6)+(5*5)+(4*2)+(3*2)+(2*8)+(1*8)=141
141 % 10 = 1
So 66522-88-1 is a valid CAS Registry Number.

66522-88-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-dioxaspiro[4.4]nonane-9-carbaldehyde

1.2 Other means of identification

Product number -
Other names 1,4-Dioxaspiro[4.4]nonane-6-carboxaldehyde

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:66522-88-1 SDS

66522-88-1Relevant academic research and scientific papers

Novel Ring Cleavage Based on Intermolecular Aldol Condensation

Nagumo, Shinji,Matsukuma, Aki,Suemune, Hiroshi,Sakai, Kiyoshi

, p. 10501 - 10510 (2007/10/02)

Ring cleavage and reconstruction via intramolecular aldol condensation followed by Grob fragmentation under acetalization conditions (BF3/ethylene glycol) was developed into a novel ring cleavage based on intermolecular aldol condensation.On the basis of

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