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1-(N-Boc-aminomethyl)-4-(aminomethyl)benzene / 1 G

Purity: 95 %
Synonym: tert-butyl 4-(aminomethyl)benzylcarbamate; Tert-butyl N-[[4-(aminomethyl)phenyl]methyl]carbamate
Molecular Formula: H2NCH2C6H4CH2NHCO2C(CH3)3
Molecular Weight: 236.31
SKU: MND-82589
CAS Number: 108468-00-4
MDL number: MFCD02683058
Note: Prices are for comparison only. Contact Sales for current pricing.
Packing size: 1 G  
43.40 EUR



Safety Information


Hazard Statements

H315
H319
H335

Precautionary Statements

P280
P264
P305 + P351 + P338
P261
P271
P302 + P352

Pictograms



Properties

Signal WordWarning
Flash Point (C)Not available
Flash Point (F)Not available
Melting Point64-68 °C (lit.)

 Product Description

1-(N-BOC-aminomethyl)-4-(aminomethyl)benzene is a chemical compound frequently employed as a building block in organic synthesis. With a BOC (tert-butyloxycarbonyl) protecting group, it facilitates controlled reactions in the creation of various organic compounds.

 

Application:

Utilized in organic chemistry, 1-(N-BOC-aminomethyl)-4-(aminomethyl)benzene serves as a crucial building block for the synthesis of diverse organic compounds, particularly in pharmaceutical and specialty chemical manufacturing.

 

 

Articles:

- Characterization of the Reduction of Oxygen at Anthraquinone-Modified Glassy Carbon and Highly Oriented Pyrolytic Graphite Electrodes

Publication Date: 11 Jul 2017

Izzet Koçak

https://doi.org/10.1080/00032719.2016.1236126

 

- A novel boronic acid-based fluorescent sensor for selectively recognizing Fe3+ ion in real time

Publication Date: 2019

Guiqian Fang, Hao Wang, Zhancun Bian, Min Guo, Zhongyu Wu and Qingqiang Yao

https://doi.org/10.1039/C9RA03978C

 

- Parallel Synthesis of an Imidazole-4,5-dicarboxamide Library Bearing Amino Acid Esters and Alkanamines

Publication Date: 15 December 2008

Rosanna Solinas, John C. DiCesare and Paul W. Baures

https://doi.org/10.3390/molecules13123149