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1,7-Naphthyridin-8(7H)-imine, 7-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

97732-16-6

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97732-16-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97732-16-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,7,3 and 2 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 97732-16:
(7*9)+(6*7)+(5*7)+(4*3)+(3*2)+(2*1)+(1*6)=166
166 % 10 = 6
So 97732-16-6 is a valid CAS Registry Number.

97732-16-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-methyl-1,7-naphthyridin-8-imine

1.2 Other means of identification

Product number -
Other names 7,8-dihydro-8-imino-7-methyl-1,7-naphthyridine

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:97732-16-6 SDS

97732-16-6Downstream Products

97732-16-6Relevant academic research and scientific papers

An Unusual Ring Contraction of 7-Methyl-1,7-naphthyridinium and 6-Methyl-1,6-naphthyridinium Salts in Reaction with Liquid Ammonia/Potassium Permanganate

Wozniak, M.,Plas, H. C. van der,Harkema, S.

, p. 3435 - 3437 (2007/10/02)

Treatment of 7-methyl-1,7-naphthyridinium iodide (1) with liquid ammonia/potassium permanganate gives the 8-imino compound 3 and two ring contraction products, which by 1H NMR spectroscopy were assigned as 3-amino-1,3-dihydro-2-methyl-4-azaisoindol-1-one (5) and 1,3-dihydro-2-methyl-4-azaisoindole-1,3-dione (6).The structure of 5 was confirmed by X-ray analysis.Similarly from 6-methyl-1,6-naphthyridinium iodide (2) the 5-imino compound 7 together with 1-amino-1,3-dihydro- (8) and 1-imino-1,3-dihydro-2-methyl-4-azaisoindol-3-one (9) were formed. 1H NMR spectroscopy unequivocally shows that 1 and 2 are converted with ammonia into 8-amino-7,8-dihydro-7-methyl-1,7-naphthyridine (11) and 5-amino-5,6-dihydro-6-methyl-1,6-naphthyridine (12), respectively.The mechanism of the ring contraction is discussed.

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