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205759-45-1

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205759-45-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 205759-45-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,5,7,5 and 9 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 205759-45:
(8*2)+(7*0)+(6*5)+(5*7)+(4*5)+(3*9)+(2*4)+(1*5)=141
141 % 10 = 1
So 205759-45-1 is a valid CAS Registry Number.

205759-45-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(3-formyl-phenyl)-phthalimide

1.2 Other means of identification

Product number -
Other names N-(3-Formyl-phenyl)-phthalimid

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:205759-45-1 SDS

205759-45-1Relevant articles and documents

Preparation of acetals from aldehydes and alcohols under basic conditions

Grabowski, Jakub,Granda, Jaros?aw M.,Jurczak, Janusz

supporting information, p. 3114 - 3120 (2018/05/17)

A new, simple protocol for the synthesis of acetals under basic conditions from non-enolizable aldehydes and alcohols has been reported. Such reactivity is facilitated by a sodium alkoxide along with a corresponding trifluoroacetate ester, utilizing formation of sodium trifluoroacetate as a driving force for acetal formation. The usefulness of this protocol is demonstrated by its orthogonality with various acid-sensitive protecting groups and by good compatibility with functional groups, delivering synthetically useful acetals complementarily to the synthesis under acidic conditions from aldehydes and alcohols.

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