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1556-22-5

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1556-22-5 Usage

Derivative of cinnolinone

A modified version of the parent compound cinnolinone, which is a bicyclic heterocyclic compound.

Common use as intermediate

Frequently used in chemical reactions to form more complex molecules in the synthesis of pharmaceuticals, agrochemicals, and various organic compounds.

Applications in synthesis

Utilized in the production of antiviral and anticancer agents, as well as in the development of insecticides and herbicides.

Building block in pharmaceutical industry

Serves as a fundamental component in creating a wide range of medicines and therapeutic agents.

Versatile nature

The compound's ability to be used in various chemical reactions and processes makes it a valuable asset in organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 1556-22-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,5 and 6 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1556-22:
(6*1)+(5*5)+(4*5)+(3*6)+(2*2)+(1*2)=75
75 % 10 = 5
So 1556-22-5 is a valid CAS Registry Number.

1556-22-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methylcinnolin-4-one

1.2 Other means of identification

Product number -
Other names 1-methylcinnolin-4(1H)-one

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:1556-22-5 SDS

1556-22-5Downstream Products

1556-22-5Relevant articles and documents

On the tautomerism of cinnolin-4-ol, cinnoline-4-thiol, and cinnolin-4-amine

Holzer, Wolfgang,Eller, Gernot A.,Schoenberger, Simeon

, p. 77 - 86 (2008/09/20)

Detailed NMR spectroscopic investigations (1H, 13C, 15N) with cinnolin-4-ol (1) reveal this compound to exist exclusively in the cinnolin-4(1H)-one form in deuteriodimethyl sulfoxide solution. This finding is confirmed by comparison of the NMR spectroscopic data of 1 with those of the corresponding 'fixed' O-methyl and N-methyl derivatives, i.e. 4-methoxycinnoline (3) and 1-methylcinnolin-4(1H)-one (5). Similarly, cinnoline-4-thiol (4) is present in the thione form in deuteriodimethyl sulfoxide, whereas cinnolin-4-amine (7) exists in the amino form. In addition, in-depth analyses of the NMR spectra of some simple 4-substituted cinnolines are provided.

Central nervous system active compounds. IX. Cinnolinylisobenzofuranones [1-(3-phthalidyl)cinnolin-4(1H)-ones]

Marshall,Mooney,Prager,Ward

, p. 2619 - 2627 (2007/10/02)

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