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502559-01-5

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502559-01-5 Usage

Molecular Weight

202.33 g/mol

Physical State

Colorless liquid

Structure

Spiro ring with four ethyl groups

Applications

a. Organic solvent
b. Potential use in pharmaceutical and chemical industries

Versatility

Facilitates various chemical reactions and synthetic processes due to its unique structure

Availability

Limited information in academic literature and industrial applications

Presence

Relatively less common in the chemical community

Check Digit Verification of cas no

The CAS Registry Mumber 502559-01-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,2,5,5 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 502559-01:
(8*5)+(7*0)+(6*2)+(5*5)+(4*5)+(3*9)+(2*0)+(1*1)=125
125 % 10 = 5
So 502559-01-5 is a valid CAS Registry Number.

502559-01-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,5,5-tetraethyl-1,6-dioxaspiro[2.4]heptane

1.2 Other means of identification

Product number -
Other names 2,2,5,7,8-PENTAMETHYLCHROMAN-6-SULFONAMIDE

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:502559-01-5 SDS

502559-01-5Downstream Products

502559-01-5Relevant articles and documents

Synthesis of substituted 1,5-dioxaspiro[2.4]heptanes from 2,3-dichloroprop-1-ene

Alonso, Francisco,Melendez, Jaisiel,Yus, Miguel

, p. 3262 - 3271 (2007/10/03)

The 4,4′-di (tert-butyl)biphenyl(DTBB)-catalyzed lithiation of 2,3-dichloroprop-1-ene (10) in THF at 0°, in the presence of symmetrically substituted ketones, led to the corresponding methylene-substituted diols 11 (Scheme 2), which, by treatment with NaH

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