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4-Nitrobenzylamine hydrochloride


  • CAS
  • Purity
  • 18600-42-5
  • 99%
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1.What is the 4-Nitrobenzylamine hydrochloride ?

4-Nitrobenzylamine hydrochloride was used in chemical modification of graphite powder and multiwalled carbon nanotubes. It was also used in the preparation of 2-fluoro-6-(4-nitrohenzylamino)purine.

4-nitrobenzonitrile
619-72-7

4-nitrobenzonitrile

4-nitrobenzylamine hydrochloride
18600-42-5

4-nitrobenzylamine hydrochloride

Conditions
Conditions Yield
4-nitrobenzonitrile; With C46H178O41Si42; titanium(IV)isopropoxide; In toluene; at 60 ℃; for 9h; Inert atmosphere;
With hydrogenchloride; water; In toluene; at 20 ℃; Reagent/catalyst; chemoselective reaction; Inert atmosphere;
90%
4-nitrobenzonitrile; With titanium(IV) isopropylate; 1,1,3,3-Tetramethyldisiloxane; In toluene; at 60 ℃; for 24h; Inert atmosphere;
With hydrogenchloride; In water; at 20 ℃;
86%
With hydrogenchloride; diborane; Multistep reaction; 2) ether;
Multi-step reaction with 2 steps
1: tris(pentafluorophenyl)borate / chloroform-d1 / 0.17 h / 85 °C / Inert atmosphere
2: hydrogenchloride; water / diethyl ether / 1 h / 20 °C
With hydrogenchloride; tris(pentafluorophenyl)borate; water; In diethyl ether; chloroform-d1;
4-nitrobenzamide
619-80-7

4-nitrobenzamide

4-nitrobenzylamine hydrochloride
18600-42-5

4-nitrobenzylamine hydrochloride

Conditions
Conditions Yield
4-nitrobenzamide; With [(aNHC)KN(SiMe3)2]2; 4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane; In toluene; at 40 ℃; for 12h; Inert atmosphere; Glovebox; Schlenk technique;
With water; sodium hydroxide; In diethyl ether; toluene; at 40 ℃; for 1h; Inert atmosphere; Glovebox; Schlenk technique;
With hydrogenchloride; In diethyl ether; water; Reagent/catalyst; chemoselective reaction; Inert atmosphere; Glovebox; Schlenk technique;
83%
4-nitrobenzamide; With bis(tetrahydrofuran)calcium di(bis(trimethylsilyl)amide); 4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane; In toluene; at 120 ℃; for 36h; Inert atmosphere; Schlenk technique;
With hydrogenchloride; In diethyl ether; toluene; Inert atmosphere; Schlenk technique;
71%
Yield given. Multistep reaction;
Multi-step reaction with 2 steps
1: lithium 2,6-di-tert-butylphenolate / neat (no solvent) / 18 h / 60 °C / Inert atmosphere; Glovebox; Schlenk technique
2: sodium hydroxide / water; diethyl ether / 1 h
With lithium 2,6-di-tert-butylphenolate; sodium hydroxide; In diethyl ether; water;
Multi-step reaction with 2 steps
1: La(CH2 C6 H4 NMe2 -o)3 on SBA-15 / toluene / 24 h / 120 °C / Schlenk technique; Inert atmosphere
2: hydrogenchloride / ethyl acetate; diethyl ether / 20 °C / Schlenk technique; Inert atmosphere
With hydrogenchloride; In diethyl ether; ethyl acetate; toluene;

2.What is the CAS number for 4-Nitrobenzylamine hydrochloride ?

The CAS number of 4-Nitrobenzylamine hydrochloride is 18600-42-5.

More information of 4-Nitrobenzylamine hydrochloride 18600-42-5 are:

CAS?Number

18600-42-5

Melting Point

~265 °C (dec.)(lit.)

Boiling Point

297.5°C at 760 mmHg

Flash Point

133.7°C

Vapor Pressure

0.00135mmHg at 25°C

HS CODE

29214990

PSA

71.84000

LogP

3.07900

3.What are another words for 4-Nitrobenzylamine hydrochloride ?

Synonyms?for?4-Nitrobenzylamine hydrochloride 18600-42-5:Benzenemethanamine,4-nitro-, monohydrochloride (9CI);Benzylamine, p-nitro-, hydrochloride(6CI,7CI);Benzylamine, p-nitro-, monohydrochloride (8CI);p-Nitrobenzylamine hydrochloride;

4.What is the molecular formula of 4-Nitrobenzylamine hydrochloride?

The chemical formula of ?4-Nitrobenzylamine hydrochloride is?C7H8N2O2. HCl which containing 7 Carbon atoms,9 Hydrogen atoms,2 Nitrogen atoms,1 Oxygen atoms and 1 Chlorine atoms,and the molecular weight of??4-Nitrobenzylamine hydrochloride?is 188.614.

5.What is 4-Nitrobenzylamine hydrochloride (18600-42-5) used for?

4-Nitrobenzylamine hydrochloride is a light brown crystalline solid that is commonly utilized in various chemical reactions and modifications due to its unique properties.

InChI:InChI=1/C7H8N2O2/c8-5-6-1-3-7(4-2-6)9(10)11/h1-4H,5,8H2/p+1

Relevant articles related to 4-Nitrobenzylamine hydrochloride:

Article

Source

Lithium compound catalyzed deoxygenative hydroboration of primary, secondary and tertiary amides

Bisai, Milan Kumar,Gour, Kritika,Das, Tamal,Vanka, Kumar,Sen, Sakya S.

, p. 2354 - 2358 (2021/03/03)

Fabrication of ω-Transaminase@Metal-Organic Framework Biocomposites for Efficiently Synthesizing Benzylamines and Pyridylmethylamines

Chen, Lina,Ding, Yingying,Jiao, Qingcai,Liu, Junzhong,Yu, Jinhai,Zhang, Hongjuan,Zong, Weilu

, (2021/11/05)

6.Buy 4-Nitrobenzylamine hydrochloride with the best price .

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