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Isoindolo[2,1-a]quinoline-5,11-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

143583-69-1

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143583-69-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 143583-69-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,5,8 and 3 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 143583-69:
(8*1)+(7*4)+(6*3)+(5*5)+(4*8)+(3*3)+(2*6)+(1*9)=141
141 % 10 = 1
So 143583-69-1 is a valid CAS Registry Number.

143583-69-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name isoindolo[2,3-a]quinoline-5,11-dione

1.2 Other means of identification

Product number -
Other names -

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:143583-69-1 SDS

143583-69-1Downstream Products

143583-69-1Relevant academic research and scientific papers

A simple synthesis of 5-(2-Aminophenyl)-1H-pyrazoles

Janjic, Monika,Prebil, Rok,Groselj, Uros,Kralj, David,Malavasic, Crt,Golobic, Amalija,Stare, Katarina,Dahmann, Georg,Stanovnik, Branko,Svete, Jurij

, p. 1703 - 1717 (2011/10/31)

A four-step synthesis of 1-substituted 5-(2-aminophenyl)-1H-pyrazoles 5 as a novel type of histamine analogs and versatile building blocks for further transformations was developed. The synthesis starts from commercially available 2-nitroacetophenone (12), which is converted into the enamino ketone 13 as the key intermediate. Cyclization of the key intermediate 13 with monosubstituted hydrazines 14a-14l afforded the 5-(2-nitrophenyl)-1H-pyrazoles 17a-17l. Finally, catalytic hydrogenation of the nitro compounds 17a, 17c-17e, and 17g-17j furnished the title compounds 5a, 5c-5e, and 5g-5j, respectively, in good yields. As demonstrated by some further transformations, additional functionalization of compounds 17 and 5 is feasible, either by electrophilic substitution at C(4) of the pyrazole ring, or at the NH2 group. Copyright

A new route to quinolone and indole skeletones via ketone- and ester-imide cyclodehydration reactions

Kim, Guncheol,Keum, Gyochang

, p. 1979 - 1988 (2007/10/03)

Ketone-imide cyclodehydration reactions of aromatic succinimide and phthalimide (7, 8) have afforded quinolone acids (11, 12). Further transformation of the acids provided the corresponding esters (13, 14) and vinylogous urethanes (9, 10). Similarly, ester-imide cyclodehydration reactions of aromatic imide esters (19, 20) have afforded indole acids (23, 24).

Spectroscopic Studies of Benzimidazole, Quinoxaline and Quinoline Derivatives.

Alkhathlan, Hamad Z.,Al-Lohedan, Hamad A.

, p. 201 - 220 (2007/10/02)

Four fused benzimidazoles, two quinoxalines and two fused quinoline derivatives were studied with respect to their MS, NMR and IR spectra.These compounds were chosen in order to compare the effect of the size of the hetero ring and the presence of C=N and C=O on their spectral behavior.

Novel Approach to Pyrroloquinoline-1,5-diones

AlKhathlan, Hamad Z.

, p. 1984 - 1996 (2007/10/02)

The condensation of 2-aminoacetophenone with acid anhydrides is investigated.Different fused 4-quinolone derivatives were prepared in one step via this condensation.In addition different N-substituted imides were also obtained.

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