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120737-77-1

1-Benzyl-4-BOC-Piperazine, systematically named 1-Benzyl-4-(tert-butoxycarbonyl)piperazine, is a specialized organic compound widely used in pharmaceutical research and development. It is characterized by the presence of a piperazine ring, a common feature in many pharmacologically active compounds. 1-BENZYL-4-BOC-PIPERAZINE is often utilized as a reagent or intermediate in the synthesis of various drug compounds, playing a critical role in the development of therapeutic pharmaceuticals.

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  • 120737-77-1 Structure

  • Basic information

    1. Product Name: 1-BENZYL-4-BOC-PIPERAZINE
    2. Synonyms: BUTTPARK 146\06-23;1-BENZYL-4-BOC-PIPERAZINE;4-BENZYL-1-T-BUTOXYCARBONYLPIPERAZINE;4-BENZYL-1-BOC-PIPERAZINE;4-BENZYL-PIPERAZINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER;TERT-BUTYL 4-BENZYL-1-PIPERAZINECARBOXYLATE;TERT-BUTYL 4-BENZYL-2-METHYLPIPERAZINE-1-CARBOXYLATE;4-Benzyl-2-methylpiperazine-1-carboxylic acid tert-butyl ester
    3. CAS NO:120737-77-1
    4. Molecular Formula: C17H26N2O2
    5. Molecular Weight: 276.37
    6. EINECS: 604-604-1
    7. Product Categories: N/A
    8. Mol File: 120737-77-1.mol

  • Chemical Properties

    1. Melting Point: 71-73 °C(lit.)
    2. Boiling Point: 371.5°Cat760mmHg
    3. Flash Point: 178.5°C
    4. Appearance: /
    5. Density: 1.059g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1-BENZYL-4-BOC-PIPERAZINE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-BENZYL-4-BOC-PIPERAZINE(120737-77-1)
    11. EPA Substance Registry System: 1-BENZYL-4-BOC-PIPERAZINE(120737-77-1)

  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: 36/37/38
    3. Safety Statements: 26-37/39
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 120737-77-1(Hazardous Substances Data)

120737-77-1 Usage

Uses

Used in Pharmaceutical Research and Development:
1-Benzyl-4-BOC-Piperazine is used as a reagent or intermediate for the synthesis of various drug compounds. Its presence in the molecular structure of many pharmacologically active compounds makes it a valuable component in the creation of therapeutic pharmaceuticals.
Used in Organic Chemistry:
As an organic compound, 1-Benzyl-4-BOC-Piperazine is also utilized in various organic chemistry applications, including the development of new chemical reactions and the synthesis of complex organic molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 120737-77-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,7,3 and 7 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 120737-77:
(8*1)+(7*2)+(6*0)+(5*7)+(4*3)+(3*7)+(2*7)+(1*7)=111
111 % 10 = 1
So 120737-77-1 is a valid CAS Registry Number.

120737-77-1 Well-known Company Product Price

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  • Alfa Aesar

  • (H33694)  4-Benzyl-1-Boc-2-methylpiperazine, 97%   

  • 120737-77-1

  • 250mg

  • 480.0CNY

  • Detail

  • Alfa Aesar

  • (H33694)  4-Benzyl-1-Boc-2-methylpiperazine, 97%   

  • 120737-77-1

  • 1g

  • 1333.0CNY

  • Detail

120737-77-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl 4-benzyl-2-methylpiperazine-1-carboxylate

1.2 Other means of identification

Product number -
Other names 4-BENZYL-2-METHYLPIPERAZINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:120737-77-1 SDS

120737-77-1Relevant articles and documents

General Procedures for the Lithiation/Trapping of N-Boc Piperazines

Firth, James D.,O'Brien, Peter,Ferris, Leigh

, p. 7023 - 7031 (2017/07/17)

To provide α-substituted piperazines for early stage medicinal chemistry studies, a simple, general synthetic approach is required. Here, we report the development of two general and simple procedures for the racemic lithiation/trapping of N-Boc piperazin

Synthesis of piperazine derivatives by Cp (*)Ir complex-catalyzed N-alkylative reactions of ethanolamines

Fujita, Ken-Ichi,Kida, Yasushi,Yamaguchi, Ryohei

experimental part, p. 1371 - 1377 (2010/10/03)

A new method for the synthesis of piperazine derivatives catalyzed by a Cp (*)Ir complex has been developed. Cp (*)Ir complex-catalyzed N-alkylative homocoupling reactions of N-benzylethanolamines give N,N'-dibenzylpiperazine derivatives. For example, the

1,4-DISUBSTITUTED PIPERAZINE AND 1,4-DISUBSTITUTED AZEPANE AS 11 -BETA-HYDROXYSTEROID DEHYDROGENASE 1 INHIBITORS

-

Page/Page column 31, (2010/11/29)

Compounds of formula (I): wherein variable groups are defined within; their use in the inhibition of 11βHSD1, processes for making them and pharmaceutical compositions comprising them are described.

N-aryl-piperazinealkanamides useful for improving sleep

-

, (2008/06/13)

A method of improving sleep in warm-blooded animals suffering from sleep disorders, which method comprises the administration of particular N-aryl-piperazinealkanamide derivatives and compositions containing the same. Novel N-aryl-piperazinealkanamide derivatives.

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