N-Boc-piperazine

Modify Date: 2024-01-02 15:57:17

N-Boc-piperazine Structure
N-Boc-piperazine structure
Common Name N-Boc-piperazine
CAS Number 57260-71-6 Molecular Weight 186.251
Density 1.0±0.1 g/cm3 Boiling Point 258.0±15.0 °C at 760 mmHg
Molecular Formula C9H18N2O2 Melting Point 47-49ºC
MSDS Chinese USA Flash Point 109.8±20.4 °C
Symbol GHS07
GHS07
Signal Word Warning

 Use of N-Boc-piperazine


N-Boc-piperazine is a Alkyl/ether-based PROTAC linker that can be used in the synthesis of PROTAC PD-1/PD-L1 degrader-1 (HY-131183)[1].

 Names

Name 1-Boc-piperazine
Synonym More Synonyms

 N-Boc-piperazine Biological Activity

Description N-Boc-piperazine is a Alkyl/ether-based PROTAC linker that can be used in the synthesis of PROTAC PD-1/PD-L1 degrader-1 (HY-131183)[1].
Related Catalog
Target

Alkyl/ether

In Vitro PROTACs contain two different ligands connected by a linker; one is a ligand for an E3 ubiquitin ligase and the other is for the target protein. PROTACs exploit the intracellular ubiquitin-proteasome system to selectively degrade target proteins[1].
References

[1]. Binbin Cheng, et al. Discovery of novel resorcinol diphenyl ether-based PROTAC-like molecules as dual inhibitors and degraders of PD-L1. Eur J Med Chem. 2020;199:112377.

 Chemical & Physical Properties

Density 1.0±0.1 g/cm3
Boiling Point 258.0±15.0 °C at 760 mmHg
Melting Point 47-49ºC
Molecular Formula C9H18N2O2
Molecular Weight 186.251
Flash Point 109.8±20.4 °C
Exact Mass 186.136826
PSA 41.57000
LogP 0.55
Vapour Pressure 0.0±0.5 mmHg at 25°C
Index of Refraction 1.467
Storage condition Refrigerator

 Safety Information

Symbol GHS07
GHS07
Signal Word Warning
Hazard Statements H315-H319-H335
Precautionary Statements P261-P305 + P351 + P338
Personal Protective Equipment dust mask type N95 (US);Eyeshields;Gloves
Hazard Codes Xi: Irritant;
Risk Phrases R36/37/38
Safety Phrases S26
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2933990090

 Synthetic Route

 Customs

HS Code 2933599090
Summary 2933599090. other compounds containing a pyrimidine ring (whether or not hydrogenated) or piperazine ring in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 Articles7

More Articles
Synthesis and dual D2 and 5-HT1A receptor binding affinities of 5-piperidinyl and 5-piperazinyl-1H-benzo[d]imidazol-2(3H)-ones.

J. Enzyme Inhib. Med. Chem. , (2013)

A series of new 5-piperidinyl and 5-piperazinyl-1H-benzo[d]imidazol-2(3H)-ones have been synthesized and evaluated for dual D2 and 5-HT1A receptor binding affinities. The synthesized ligands are struc...

Design, synthesis and structure-activity relationship studies of novel indazole analogues as DNA gyrase inhibitors with Gram-positive antibacterial activity.

Bioorg. Med. Chem. Lett. 14 , 2857-2862, (2004)

In this study, we report the design, synthesis and structure-activity relationships of novel indazole derivatives as DNA gyrase inhibitors with Gram-positive antibacterial activity. Our results show t...

Molecular iodine-catalyzed facile procedure for N-Boc protection of amines.

J. Org. Chem. 71 , 8283, (2006)

An efficient and practical protocol for the protection of various structurally and electronically divergent aryl and aliphatic amines using (Boc)2O in the presence of a catalytic amount of molecular i...

 Synonyms

piperazine-1-carboxylic acid tert-butyl ester
1-Piperazinecarboxylic acid, 1,1-dimethylethyl ester
BOC-PIPERAZINE
2-Methyl-2-propanyl 1-piperazinecarboxylate
1-Boc piperzine
t-Butyl 1-piperazincarboxylate
tert-butyl piperazine-1-carboxylate
1,1-Dimethylethyl 1-piperazinecarboxylate
1-BOC-Piperazine
PIBOC
MFCD00075265
tert-butyl tetrahydropyrazine-1(2H)-carboxylate
N-BOC-PIPERAZINE
tert-butyl l-piperazinecarboxylate
1-N-BOC-PIPERAZINE
RARECHEM AR PA 0026
BOC-PAZ
N-Boc-piperazine; tert-butyl piperazine-1-carboxylate
tert-Butyl 1-piperazinecarboxylate
N-Boc-piperazine
N Boc-Piperazine
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