Intermediate of API

10269-01-9

  • Product Name：3-Bromobenzylamine
  • Molecular Formula：C7H8BrN
  • Specifications：99%
  • Molecular Weight：186.051
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Product Details;

CasNo： 10269-01-9

Molecular Formula： C7H8BrN

Appearance： clear yellow liquid

Reliable Quality 3-Bromobenzylamine 10269-01-9 For Sale with Best Price

  • Molecular Formula:C7H8BrN
  • Molecular Weight:186.051
  • Appearance/Colour:clear yellow liquid 
  • Vapor Pressure:0.0303mmHg at 25°C 
  • Refractive Index:1.584-1.586  
  • Boiling Point:244.499 °C at 760 mmHg 
  • PKA:8.77±0.10(Predicted) 
  • Flash Point:104.347 °C 
  • PSA：26.02000 
  • Density:1.481 g/cm3 
  • LogP:2.60810 

3-Bromobenzylamine(Cas 10269-01-9) Usage

Chemical Properties

clear yellow liquid

Uses

3-Bromobenzylamine, a potential inhibitor of the host ACE2 protein, is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agro chemicals, dyestuff.

InChI:InChI=1/C7H8BrN/c8-7-3-1-2-6(4-7)5-9/h1-4H,5,9H2

10269-01-9 Relevant articles

Discovery of dually acting small-molecule inhibitors of cancer-resistance relevant receptor tyrosine kinases EGFR and IGF-1R

Hempel, Cornelius,Najjar, Abdulkarim,Totzke, Frank,Sch?chtele, Christoph,Sippl, Wolfgang,Ritter, Christoph,Hilgeroth, Andreas

, p. 2159 - 2166 (2016)

Novel benzo-anellated furo- and pyrrolo[...

Reaction of Diisobutylaluminum Borohydride, a Binary Hydride, with Selected Organic Compounds Containing Representative Functional Groups

Amberchan, Gabriella,Snelling, Rachel A.,Moya, Enrique,Landi, Madison,Lutz, Kyle,Gatihi, Roxanne,Singaram, Bakthan

supporting information, p. 6207 - 6227 (2021/05/06)

The binary hydride, diisobutylaluminum b...

Comparative account of catalytic activity of Ru- and Ni-based nanocomposites towards reductive amination of biomass derived molecules

Bhanage, Bhalchandra M.,Gokhale, Tejas A.,Raut, Amol B.

, (2021/06/18)

This work includes an effective comparis...

Synthesis and antimicrobial activity of some 3-substituted benzylamines

B. R. K. Menon, K. L. K. M. Rao, and N. G. R. Nair

, Journal of Chemistry, vol. 12, pp. 108-110, 1974

The antimicrobial activity of the compounds was evaluated against several bacterial and fungal strains, and it was found that some of the compounds exhibited significant activity against certain strains. Overall, the authors conclude that the 3-substituted benzylamines synthesized in this study have potential as antimicrobial agents.

Rewritable Macromolecular Data Storage with Automated Read‐out

M Soete, K De Bruycker, F Du Prez

, Angewandte Chemie, 2022

For this, the thiolactone end-groups of the oligomers were first ring-opened by using 3-bromobenzylamine.

10269-01-9 Process route

N-m-bromobenzyl-2,2,6,6-tetramethylpiperidin-4-ol

N-m-bromobenzyl-2,2,6,6-tetramethylpiperidin-4-ol

phorone
504-20-1

phorone

3-bromobenzylamine
10269-01-9

3-bromobenzylamine

Conditions
Conditions Yield
Multi-step reaction with 2 steps
1: C20H29ClO2P2Pt; 1-Phenylbut-1-en-3-one; sodium hydroxide / toluene / 4 h / 105 °C
2: hydrogenchloride / 5 h / 105 °C
With hydrogenchloride; C20H29ClO2P2Pt; 1-Phenylbut-1-en-3-one; sodium hydroxide; In toluene;
 
C<sub>16</sub>H<sub>22</sub>BrNO

C16H22BrNO

phorone
504-20-1

phorone

3-bromobenzylamine
10269-01-9

3-bromobenzylamine

Conditions
Conditions Yield
With hydrogenchloride; at 105 ℃; for 5h;
 

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