Ethyl N-piperazinecarboxylate

  • CasNo：120-43-4
  • purity：99%
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1.What is the Ethyl N-piperazinecarboxylate ?

Intermediate.

piperazine
110-85-0

piperazine

chloroformic acid ethyl ester
541-41-3

chloroformic acid ethyl ester

4-ethoxycarbonylpiperazine
120-43-4

4-ethoxycarbonylpiperazine

Conditions
Conditions Yield
In methanol; water; at 0 - 25 ℃; for 4h;
33.7%
In methanol; water; at 0 - 25 ℃; for 4h;
33.7%
bei pH 2.8-4.6;
With ethanol;
With water;
In chloroform; at 1 - 20 ℃; for 3h;
methyl 4-benzylpiperazine-1-carboxylate

methyl 4-benzylpiperazine-1-carboxylate

4-ethoxycarbonylpiperazine
120-43-4

4-ethoxycarbonylpiperazine

Conditions
Conditions Yield
With palladium 10% on activated carbon; hydrogen; In methanol; at 40 ℃; for 48h;

2.What is the CAS number for Ethyl N-piperazinecarboxylate ?

The CAS number of Ethyl N-piperazinecarboxylate is 120-43-4.

More information of Ethyl N-piperazinecarboxylate 120-43-4 are:

CAS?Number

120-43-4

Density

1.071 g/cm3

Melting Point

120 °C

Boiling Point

237 °C at 760 mmHg

Flash Point

97.1 °C

Vapor Pressure

0.0459mmHg at 25°C

Refractive Index

n20/D 1.477(lit.)

HS CODE

29335995

PSA

41.57000

LogP

0.31480

Pka

8.50±0.10(Predicted)

3.What are another words for Ethyl N-piperazinecarboxylate ?

Synonyms?for?Ethyl N-piperazinecarboxylate 120-43-4:1-(Ethoxycarbonyl)piperazine;1-Carbethoxypiperazine;1-Carboethoxypiperazine;4-Carbethoxypiperazine;Ethyl1-piperazinecarboxylate;N-(Ethoxycarbonyl)piperazine;N-Carbethoxypiperazine;N-Carboethoxypiperazine;NSC 21060;NSC 22134;NSC 280827;

4.What is the molecular formula of Ethyl N-piperazinecarboxylate?

The chemical formula of ?Ethyl N-piperazinecarboxylate is?C7H14N2O2 which containing 7 Carbon atoms,14 Hydrogen atoms,2 Nitrogen atoms and 2 Oxygen atoms,and the molecular weight of??Ethyl N-piperazinecarboxylate?is 158.2.

5.What is Ethyl N-piperazinecarboxylate (120-43-4) used for?

InChI:InChI=1/C7H14N2O2/c1-2-11-7(10)9-5-3-8-4-6-9/h8H,2-6H2,1H3/p+1

Relevant articles related to Ethyl N-piperazinecarboxylate:

Article

Source

-

Das et al.

, p. 890 (1971)

Heteroaryl substituted dihydro pyrimidine compounds and their use in medicine

-

Paragraph 0458; 0461; 0462, (2018/02/23)

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