74316-55-5

  • Product Name:5-Bromo-8-methylquinoline
  • Molecular Formula:C10H8BrN
  • Purity:99%
  • Molecular Weight:222.084
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Product Details;

CasNo: 74316-55-5

Molecular Formula: C10H8BrN

factory and supplier 74316-55-5 5-Bromo-8-methylquinoline in stock

  • Molecular Formula:C10H8BrN
  • Molecular Weight:222.084
  • Melting Point:37-38 °C 
  • Boiling Point:315.7±22.0 °C(Predicted) 
  • PKA:3.95±0.29(Predicted) 
  • PSA:12.89000 
  • Density:1.488±0.06 g/cm3(Predicted) 
  • LogP:3.30570 

74316-55-5 Relevant articles

Three-Component Couplings among Heteroarenes, Difluorocyclopropenes, and Water via C-H Activation

Liu, Xuexin,Chen, Jian,Yang, Chunyan,Wu, Zhouping,Li, Zhiyang,Shi, Yuesen,Huang, Tianle,Yang, Zhongzhen,Wu, Yong

supporting information, p. 6831 - 6835 (2021/09/08)

Three-component couplings have been real...

RhIII-Catalyzed Direct Heteroarylation of C(sp3)-H and C(sp2)-H Bonds in Heterocycles with N-Heteroaromatic Boronates

Wang, Huai-Wei,Wu, Jia-Xue,Qiao, Yu-Han,Li, Yong-Fei,Li, Da-Cheng,Dou, Jian-Min,Yao, Qing-Xia,Lu, Yi

supporting information, p. 7177 - 7182 (2021/09/18)

Herein, we disclose a RhIII-catalyzed he...

1H-PYRAZOLO[4,3-d]PYRIMIDINE COMPOUNDS AS TOLL-LIKE RECEPTOR 7 (TLR7) AGONISTS

-

Paragraph 00140-00141, (2021/08/06)

Compounds according to formula I are use...

Rh(iii)-Catalyzed straightforward arylation of 8-methyl/formylquinolines using diazo compounds

Ghosh, Bidhan,Samanta, Rajarshi

supporting information, p. 6886 - 6889 (2019/06/18)

A straightforward Rh(iii)-catalyzed gene...

74316-55-5 Process route

8-methylquinoline
611-32-5

8-methylquinoline

5-bromo-8-methyl-quinoline
74316-55-5

5-bromo-8-methyl-quinoline

Conditions
Conditions Yield
With bromine; silver sulfate; In sulfuric acid; for 0.5h;
86%
With sulfuric acid; bromine; silver sulfate; at 20 ℃; for 0.5h;
86%
With sulfuric acid; bromine; silver sulfate; at 0 - 25 ℃; for 4h;
84%
With sulfuric acid; bromine; silver sulfate; at 20 ℃; for 5h;
71%
With sulfuric acid; bromine; silver sulfate; at 20 ℃; for 5h;
71%
With sulfuric acid; bromine; silver sulfate; at 20 ℃; for 0.5h;
70%
With N-Bromosuccinimide; In sulfuric acid; at 20 ℃; for 3h;
58%
With sulfuric acid; bromine; silver sulfate; In water; at 0 - 20 ℃; for 4h;
With N-Bromosuccinimide; sulfuric acid; at 5 ℃; for 18h;
8-methylquinoline; With N-Bromosuccinimide; sulfuric acid; at 5 ℃; for 18h;
With sodium hydroxide; In water;
5-bromo-2-methylaniline
39478-78-9

5-bromo-2-methylaniline

glycerol
56-81-5,25618-55-7,64333-26-2,8013-25-0

glycerol

5-bromo-8-methyl-quinoline
74316-55-5

5-bromo-8-methyl-quinoline

Conditions
Conditions Yield
With sulfuric acid; nitrobenzene;
5-bromo-2-methylaniline; glycerol; With sulfuric acid; nitrobenzene; In water; at 150 ℃; for 3h;
With sodium hydroxide; In water; at 0 ℃;
With sulfuric acid; sodium iodide; In water; at 140 - 145 ℃; for 4h; Inert atmosphere; Schlenk technique;
With sulfuric acid; sodium iodide; In water; at 140 - 145 ℃; for 4h; Schlenk technique;
With sulfuric acid; sodium iodide; In water; at 140 - 145 ℃; for 2.5h; Inert atmosphere; Schlenk technique;
With sulfuric acid; sodium iodide; at 140 ℃; for 6h;
With sulfuric acid; sodium iodide; In water; at 140 - 145 ℃; for 3.5h;
With sulfuric acid; In nitrobenzene; at 150 ℃; for 3h;
With sulfuric acid; sodium iodide; at 140 - 145 ℃; for 3.5h;
With sulfuric acid; sodium iodide; In water; at 140 - 145 ℃; for 6h;

74316-55-5 Upstream products

  • 39478-78-9
    39478-78-9

    5-bromo-2-methylaniline

  • 56-81-5
    56-81-5

    glycerol

  • 611-32-5
    611-32-5

    8-methylquinoline

  • 7726-95-6
    7726-95-6

    bromine

74316-55-5 Downstream products

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    74316-57-7

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    8-methyl-5-quinolinecarboxylic acid

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    8-[bis(benzenesulfonyl)aminomethyl]-5-bromoquinoline

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    N-[(5-bromoquinolin-8-yl)methyl]-4-methylbenzenesulfonamide

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