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205692-62-2

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205692-62-2 Usage

Chemical Properties

light yellow crystals

Check Digit Verification of cas no

The CAS Registry Mumber 205692-62-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,5,6,9 and 2 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 205692-62:
(8*2)+(7*0)+(6*5)+(5*6)+(4*9)+(3*2)+(2*6)+(1*2)=132
132 % 10 = 2
So 205692-62-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H14N2O/c1-8-7-11(12)9(10-8)5-3-2-4-6-9/h7H,2-6H2,1H3

205692-62-2SDS

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 2-methyl-4-oxido-1-aza-4-azoniaspiro[4.5]deca-1,3-diene

1.2 Other means of identification

Product number -
Other names 3-methyl-1,4-diazaspiro[4.5]deca-1,3-dien-1-ol

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:205692-62-2 SDS

205692-62-2Downstream Products

205692-62-2Relevant articles and documents

Metal-Free C-H/C-H Coupling of 2 H-Imidazole 1-Oxides with Polyphenols toward Imidazole-Linked Polyphenolic Compounds

Moseev, Timofey D.,Nikiforov, Egor A.,Varaksin, Mikhail V.,Charushin, Valery N.,Chupakhin, Oleg N.

, p. 13702 - 13710 (2021/10/01)

The methodology of nucleophilic substitution of hydrogen (SNH) was successfully applied as a convenient synthetic tool to afford azaheterocyclic derivatives of phenols of various architectures. A series of 26 novel imidazole-linked polyphenolic compounds were first prepared in 72-95% yields through the direct metal-free C-H/C-H coupling of polyphenols with 2H-imidazole 1-oxides. Comprehensive studies on the reaction condition optimization, scope, and limitations enabled the development of a straightforward method toward novel bifunctional derivatives bearing both phenolic and imidazole scaffolds of particular interest in the design of challenging molecules for versatile applications in medicinal chemistry and materials science.

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