Boc-NH-C4-Br

Modify Date: 2024-01-11 19:54:31

Boc-NH-C4-Br Structure
Boc-NH-C4-Br structure
Common Name Boc-NH-C4-Br
CAS Number 164365-88-2 Molecular Weight 252.149
Density 1.2±0.1 g/cm3 Boiling Point 308.8±25.0 °C at 760 mmHg
Molecular Formula C9H18BrNO2 Melting Point N/A
MSDS Chinese USA Flash Point 140.5±23.2 °C
Symbol GHS05
GHS05
Signal Word Danger

 Use of Boc-NH-C4-Br


Boc-NH-C4-Br is an alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs[1].

 Names

Name tert-butyl N-(4-bromobutyl)carbamate
Synonym More Synonyms

 Boc-NH-C4-Br Biological Activity

Description Boc-NH-C4-Br is an alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs[1].
Related Catalog
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]. Hu R, et, al. Identification of a selective BRD4 PROTAC with potent antiproliferative effects in AR-positive prostate cancer based on a dual BET/PLK1 inhibitor. Eur J Med Chem. 2022 Jan 5;227:113922.

 Chemical & Physical Properties

Density 1.2±0.1 g/cm3
Boiling Point 308.8±25.0 °C at 760 mmHg
Molecular Formula C9H18BrNO2
Molecular Weight 252.149
Flash Point 140.5±23.2 °C
Exact Mass 251.052078
PSA 38.33000
LogP 2.78
Vapour Pressure 0.0±0.7 mmHg at 25°C
Index of Refraction 1.473
Storage condition 2-8°C

 Safety Information

Symbol GHS05
GHS05
Signal Word Danger
Hazard Statements H318
Precautionary Statements P280-P305 + P351 + P338
Personal Protective Equipment Eyeshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter
Hazard Codes Xi: Irritant;
Risk Phrases R41
Safety Phrases S26-S39
RIDADR NONH for all modes of transport
HS Code 2924199090

 Synthetic Route

~98%

Boc-NH-C4-Br Structure

Boc-NH-C4-Br

CAS#:164365-88-2

Literature: Simonin, Jonathan; Vernekar, Sanjeev Kumar V.; Thompson, Andrew J.; Hothersall, J. Daniel; Connolly, Christopher N.; Lummis, Sarah C.R.; Lochner, Martin Bioorganic and Medicinal Chemistry Letters, 2012 , vol. 22, # 2 p. 1151 - 1155

~75%

Boc-NH-C4-Br Structure

Boc-NH-C4-Br

CAS#:164365-88-2

Literature: Bianco, Armandodoriano; Bonadies, Francesco; Napolitano, Raffaella; Ortaggi, Giancarlo Organic Preparations and Procedures International, 2004 , vol. 36, # 2 p. 141 - 149

~89%

Boc-NH-C4-Br Structure

Boc-NH-C4-Br

CAS#:164365-88-2

Literature: Berree, Fabienne; Bazureau, Jean-Pierre; Michelot, Gwendal; Le Corre, Maurice Synthetic Communications, 1999 , vol. 29, # 15 p. 2685 - 2693

~66%

Boc-NH-C4-Br Structure

Boc-NH-C4-Br

CAS#:164365-88-2

Literature: Henig, Joerg; Mamedov, Ilgar; Fouskova, Petra; Toth, Eva; Logothetis, Nikos K.; Angelovski, Goran; Mayer, Hermann A. Inorganic Chemistry, 2011 , vol. 50, # 14 p. 6472 - 6481

~%

Boc-NH-C4-Br Structure

Boc-NH-C4-Br

CAS#:164365-88-2

Literature: Journal of the Chemical Society, Perkin Transactions 2, , # 5 p. 923 - 927

~%

Boc-NH-C4-Br Structure

Boc-NH-C4-Br

CAS#:164365-88-2

Literature: Synthetic Communications, , vol. 29, # 15 p. 2685 - 2693

~%

Boc-NH-C4-Br Structure

Boc-NH-C4-Br

CAS#:164365-88-2

Literature: Kim, Tae Woo; Park, Jung-hyun; Hong, Jong-In Journal of the Chemical Society, Perkin Transactions 2, 2002 , # 5 p. 923 - 927

 Customs

HS Code 2924199090
Summary 2924199090. other acyclic amides (including acyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

 Articles2

More Articles
H. Ina et al.

J. Org. Chem. 61 , 1023 , (1995)

D.L. Selwood et al.

J. Med. Chem. 4 , 78, (2001)

 Synonyms

4-bromobutylamine tert-butylcarbamate
N-Boc 4-bromobutan-1-amine
tert-butyl 4-bromobutylcarbamate
Carbamic acid, N-(4-bromobutyl)-, 1,1-dimethylethyl ester
BrCH2CH2CH2CH2NHBoc
2-Methyl-2-propanyl (4-bromobutyl)carbamate
MFCD06201020
N-(4-Bromobutyl)-Carbamic Acid 1,1-Dimethylethyl Ester
tert-Butyl (4-bromobutyl)carbamate
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