NH2-C6-NH-Boc structure
|
Common Name | NH2-C6-NH-Boc | ||
---|---|---|---|---|
CAS Number | 51857-17-1 | Molecular Weight | 216.320 | |
Density | 1.0±0.1 g/cm3 | Boiling Point | 325.3±25.0 °C at 760 mmHg | |
Molecular Formula | C11H24N2O2 | Melting Point | N/A | |
MSDS | Chinese USA | Flash Point | 150.5±23.2 °C | |
Symbol |
GHS05 |
Signal Word | Danger |
Use of NH2-C6-NH-BocNH2-C6-NH-Boc is a PROTAC linker which refers to the alkyl/ether composition. NH2-C6-NH-Boc can be used in the synthesis the Mcl-1 inhibitor based on PROTAC[1]. |
Name | N-tert-Butoxycarbonyl-1,6-hexanediamine |
---|---|
Synonym | More Synonyms |
Description | NH2-C6-NH-Boc is a PROTAC linker which refers to the alkyl/ether composition. NH2-C6-NH-Boc can be used in the synthesis the Mcl-1 inhibitor based on PROTAC[1]. |
---|---|
Related Catalog | |
References |
Density | 1.0±0.1 g/cm3 |
---|---|
Boiling Point | 325.3±25.0 °C at 760 mmHg |
Molecular Formula | C11H24N2O2 |
Molecular Weight | 216.320 |
Flash Point | 150.5±23.2 °C |
Exact Mass | 216.183777 |
PSA | 64.35000 |
LogP | 1.82 |
Vapour Pressure | 0.0±0.7 mmHg at 25°C |
Index of Refraction | 1.460 |
Symbol |
GHS05 |
---|---|
Signal Word | Danger |
Hazard Statements | H314 |
Precautionary Statements | P280-P305 + P351 + P338-P310 |
Personal Protective Equipment | Faceshields;full-face respirator (US);Gloves;Goggles;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter |
Hazard Codes | C:Corrosive; |
Risk Phrases | R34 |
Safety Phrases | S26-S36/37/39-S45 |
RIDADR | UN 2735 8/PG 2 |
WGK Germany | 3 |
Packaging Group | III |
Hazard Class | 8 |
HS Code | 2924199090 |
Precursor 10 | |
---|---|
DownStream 7 | |
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% |
Carboxymethylcellulose-tetrahydrocurcumin conjugates for colon-specific delivery of a novel anti-cancer agent, 4-amino tetrahydrocurcumin.
Eur. J. Pharm. Biopharm. 88(2) , 351-60, (2014) Several curcumin derivatives are now becoming increasingly of interest because of their bioactive attributes, especially their action as antioxidants and anti-carcinogenic activities. Tetrahydrocurcum... |
|
Structure-activity relationships of novel vasopressin antagonists containing C-terminal diaminoalkanes and (aminoalkyl)guanidines.
J. Med. Chem. 32 , 391, (1989) We report the synthesis and biological activity of a series of analogues of the vasopressin antagonists [Pmp1,D-Tyr(Et)2,Val4]arginine-vasopressin (1) and [Pmp1,D-Tyr(Et)2,Val4,desGly9]arginine-vasopr... |
|
O. Buchardt et al.
J. Org. Chem. 49 , 4123, (1984)
|
N-(tert-Butoxycarbonyl)-1,6-diaminohexane |
N-Boc-1,6-hexanediamine |
tert-Butyl (6-aminohexyl)carbamate |
N-Boc-1,6-Diaminohexane |
N-(6-Aminohexyl)carbamic Acid tert-Butyl Ester |
tert-butyl N-(6-aminohexyl)carbamate |
Carbamic acid, N-(6-aminohexyl)-, 1,1-dimethylethyl ester |
MFCD00671489 |
2-Methyl-2-propanyl (6-aminohexyl)carbamate |
N-(tert-Butoxycarbonyl)-1,6-hexanediamine |