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24953-56-8

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24953-56-8 Usage

Uses

1-Methoxyphthalazine is a useful anti-corrosion agent.

Check Digit Verification of cas no

The CAS Registry Mumber 24953-56-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,9,5 and 3 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 24953-56:
(7*2)+(6*4)+(5*9)+(4*5)+(3*3)+(2*5)+(1*6)=128
128 % 10 = 8
So 24953-56-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H8N2O/c1-12-9-8-5-3-2-4-7(8)6-10-11-9/h2-6H,1H3

24953-56-8SDS

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 1-Methoxyphthalazine

1.2 Other means of identification

Product number -
Other names Phthalazine,1-methoxy

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:24953-56-8 SDS

24953-56-8Relevant articles and documents

Cu(II)-Catalyzed Construction of Heterobiaryls using 1-Diazonaphthoquinones: A General Strategy for the Synthesis of QUINOX and Related P,N Ligands

Biswas, Aniruddha,Pan, Subarna,Samanta, Rajarshi

supporting information, p. 1631 - 1636 (2022/03/14)

An efficient and straightforward method was developed for the synthesis of heterobiaryls using easily available N-oxides and diazonaphthoquinones under cheap Cu(II) catalysis. The developed method offered QUINOX and related congeners in a simple manner. A wide scope of important heterobiaryls was achieved with high site selectivity. The synthesized naphthols were transformed into the privileged related P,N ligands. Suitable resolution methods can directly afford the corresponding axially chiral heterobiaryls.

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