Catalog No.:AA00EBLA

590417-55-3 | 4-Bromo-1-methyl-1H-indole

Name: Name:4-Bromo-1-methyl-1H-indole
Brand: AABLOCKS
SKU: AA00EBLA
Availability: InStock
Rating: 90 (10 reviews)

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10g

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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:

AA00EBLA

Chemical Name:

4-Bromo-1-methyl-1H-indole

CAS Number:

590417-55-3

Molecular Formula:

C9H8BrN

Molecular Weight:

210.0705

MDL Number:

MFCD08435875

SMILES:

Brc1cccc2c1ccn2C

Properties

BP:

300.878 °C at 760 mmHg

Form:

Liquid

Refractive Index:

1.636

Storage:

Keep in dry area;2-8℃;

Computed Properties

Complexity:

149

Covalently-Bonded Unit Count:

Heavy Atom Count:

XLogP3:

2.7

Downstream Synthesis Route

590417-55-3

108-94-1

866721-35-9

[1]Baudoux,Jerome;Blake,AlexanderJ.;Simpkins,NigelS.[OrganicLetters,2005,vol.7,#19,p.4087-4089]

590417-55-3

597540-82-4

(10S,11R,14S,15S)-5,13-diaza-14-isopropyl-5-methyl-16-methylene-10-phenyl-13-(2,4,6-trimethylphenylsulfonyl)tetracyclo7.7.0.02,6.011,15hexadeca-1(9),2(6),3,7-tetraene

(10S,11S,14S,15S)-5,13-diaza-14-isopropyl-5-methyl-16-methylene-10-phenyl-13-(2,4,6-trimethylphenylsulfonyl)tetracyclo7.7.0.02,6.011,15hexadeca-1(9),2(6),3,7-tetraene

[1]Ohno,Hiroaki;Miyamura,Kumiko;Mizutani,Tsuyoshi;Kadoh,Yoichi;Takeoka,Yusuke;Hamaguchi,Hisao;Tanaka,Tetsuaki[Chemistry-AEuropeanJournal,2005,vol.11,#12,p.3728-3741]

52488-36-5

74-88-4

590417-55-3

[1]Locationinpatent:schemeortableZhou,Nian;Zeller,Wayne;Zhang,Jun;Onua,Emmanuel;Kiselyov,AlexS.;Ramirez,Jose;Palsdottir,Gudrun;Halldorsdottir,Gudrun;Andresson,Thorkell;Gurney,MarkE.;Singh,Jasbir[BioorganicandMedicinalChemistryLetters,2009,vol.19,#5,p.1528-1531]

[2]Zheng,Hong-Xing;Shan,Xiang-Huan;Qu,Jian-Ping;Kang,Yan-Biao[OrganicLetters,2017,vol.19,#19,p.5114-5117]

[3]Liu,Haichao;Chen,Lijun;Yuan,Kuo;Jia,Yanxing[AngewandteChemie-InternationalEdition,2019,vol.58,#19,p.6362-6365][Angew.Chem.,2019,vol.131,p.6428-6431,4]

[4]Rafferty,RyanJ.;Williams,RobertM.[TetrahedronLetters,2011,vol.52,#17,p.2037-2040]

[5]Stadlwieser,JosefF.;Dambaur,MarkusE.[HelveticaChimicaActa,2006,vol.89,#5,p.936-946]

[6]Despotopoulou,Christina;McKeon,SeanC.;Connon,Robert;Coeffard,Vincent;Müller-Bunz,Helge;Guiry,PatrickJ.[EuropeanJournalofOrganicChemistry,2017,vol.2017,#45,p.6734-6738]

[7]Ji,Yuan-Zhao;Li,Hui-Jing;Zhang,Jin-Yu;Wu,Yan-Chao[ChemicalCommunications,2019,vol.55,#79,p.11864-11867]

[8]Ji,Yuan-Zhao;Li,Hui-Jing;Wang,Yi-Ruo;Wu,Yan-Chao;Zhang,Zheng-Yan[Advancedsynthesisandcatalysis,2020]

[9]CurrentPatentAssignee:SIHUANPHARMACEUTICALHOLDINGSGROUPLTD.-WO2019/10295,2019,A1Locationinpatent:Page/Pagecolumn163

[10]CurrentPatentAssignee:NAVITORPHARMACEUTICALS-WO2018/191146,2018,A1Locationinpatent:Paragraph00653

[11]Tolnai,GergelyL.;Székely,Anna;Makó,Zita;Gáti,Tamás;Daru,János;Bihari,Tamás;Stirling,András;Novák,Zoltán[ChemicalCommunications,2015,vol.51,#21,p.4488-4491]

[12]CurrentPatentAssignee:ASAHIKASEICORPORATION-US2004/44258,2004,A1Locationinpatent:Page77

[13]CurrentPatentAssignee:AMGENINC-WO2006/44415,2006,A2Locationinpatent:Page/Pagecolumn87

[14]Xing,Qi;Shi,Lijun;Lang,Rui;Xia,Chungu;Li,Fuwei[ChemicalCommunications,2012,vol.48,#89,p.11023-11025]

[15]Wang,Qiang;Qi,Zisong;Xie,Fang;Li,Xingwei[AdvancedSynthesisandCatalysis,2015,vol.357,#2-3,p.355-360]

[16]Yan,Guobing;Cao,Xihan;Zheng,Wanbin;Ke,Qiumin;Zhang,Jieyu;Huang,Dayun[OrganicandBiomolecularChemistry,2017,vol.15,#28,p.5904-5907]

[17]Shen,Chaoren;Fink,Cornel;Laurenczy,Gabor;Dyson,PaulJ.;Wu,Xiao-Feng[ChemicalCommunications,2017,vol.53,#92,p.12422-12425]

[18]Duan,Shengguo;Zhang,Wan;Hu,Yuntong;Xu,Ze-Feng;Li,Chuan-Ying[AdvancedSynthesisandCatalysis,2020,vol.362,#17,p.3570-3575]

[19]Duan,Shengguo;Xue,Bing;Meng,Hui;Ye,Zihang;Xu,Ze-Feng;Li,Chuan-Ying[ChineseJournalofChemistry,2021,vol.39,#5,p.1145-1152]

590417-55-3

4,4,5,5-tetramethyl-1,3,2-dioxaborolane

1-methyl-4-(4,4,5,5-tetramethyl-1,3,2dioxaborolan-2-yl)-1H-indole

[1]Stadlwieser,JosefF.;Dambaur,MarkusE.[HelveticaChimicaActa,2006,vol.89,#5,p.936-946]

590417-55-3

866721-32-6

[1]Baudoux,Jerome;Blake,AlexanderJ.;Simpkins,NigelS.[OrganicLetters,2005,vol.7,#19,p.4087-4089]

Literature

Title: Palladium(0)-catalyzed tandem cyclization of allenenes: direct construction of tricyclic heterocycles through aromatic C--H activation.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany) 20050606

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