Catalog No.:AA00IMHM

52372-39-1 | 7H-[1]Benzopyrano[3',2':3,4]pyrido[1,2-a]benzimidazole-6-carbonitrile,3-(diethylamino)-7-imino-

Name: Name:7H-[1]Benzopyrano[3',2':3,4]pyrido[1,2-a]benzimidazole-6-carbonitrile,3-(diethylamino)-7-imino-
Brand: AABLOCKS
SKU: AA00IMHM
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>98.0%(HPLC)(N)

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Technical Information
Properties
Downstream Synthesis Route
Literature
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Technical Information
Properties
Downstream Synthesis Route
Literature

Technical Information

Catalog Number:

AA00IMHM

Chemical Name:

7H-[1]Benzopyrano[3',2':3,4]pyrido[1,2-a]benzimidazole-6-carbonitrile,3-(diethylamino)-7-imino-

CAS Number:

52372-39-1

Molecular Formula:

C23H19N5O

Molecular Weight:

381.4299

MDL Number:

MFCD02176212

SMILES:

CCN(c1ccc2c(c1)oc1c(c2)c2nc3c(n2c(=N)c1C#N)cccc3)CC

Properties

Computed Properties

Complexity:

803

Covalently-Bonded Unit Count:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Hydrogen Bond Donor Count:

Rotatable Bond Count:

XLogP3:

3.8

Downstream Synthesis Route

17754-91-5

109-77-3

52372-39-1

[1]CurrentPatentAssignee:ARAMCO(in:SaudiArabiaGovernment);GOVERNMENTOFSAUDIARABIA;SABIC(in:SaudiArabiaGovernment)-US2007/238817,2007,A1Locationinpatent:Page/Pagecolumn7

[2]Ibrayev,N.Kh.;Seliverstova;Alekseeva;Marinina;Savvina[RussianJournalofPhysicalChemistry,2013,vol.87,#7,p.1234-1238][Zh.Fiz.Khim.,2013,vol.87,#7,p.1249-1254,6]

52372-39-1

97404-16-5

9,10,10-trioxo-9,10-dihydro-1016-thioxanthene-3-carboxylicacid(6-cyano-9-diethylamino-7-oxa-4-b,13-diaza-indeno2,1-aanthracen-5-ylidene)-amide

[1]CurrentPatentAssignee:ARAMCO(in:SaudiArabiaGovernment);GOVERNMENTOFSAUDIARABIA;SABIC(in:SaudiArabiaGovernment)-US2007/238817,2007,A1Locationinpatent:Page/Pagecolumn7

52372-39-1

potassiumcyanide

C24H20N6O

[1]Locationinpatent:experimentalpartHuang,Sheng-Tung;Jian,Jia-Liang;Peng,Huai-Zu;Wang,Kun-Li;Lin,Chun-Mao;Huang,Chih-Hung;Yang,ThomasC.-K.[DyesandPigments,2010,vol.86,#1,p.6-14]

52372-39-1

10130-89-9

1227043-19-7

[1]DyesandPigments,2010,vol.86,p.6-14

Literature

Title: In vivo imaging of zebrafish retinal cells using fluorescent coumarin derivatives.

Journal: BMC neuroscience 20100101

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SDS