Boc-6-aminohexanoic acid structure
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Common Name | Boc-6-aminohexanoic acid | ||
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CAS Number | 6404-29-1 | Molecular Weight | 231.289 | |
Density | 1.1±0.1 g/cm3 | Boiling Point | 380.3±25.0 °C at 760 mmHg | |
Molecular Formula | C11H21NO4 | Melting Point | 35-40 °C | |
MSDS | USA | Flash Point | 183.8±23.2 °C |
Use of Boc-6-aminohexanoic acidBoc-6-aminohexanoic acid is an alkyl/ether-based PROTAC linker that can be used in the synthesis of PROTACs[1]. |
Name | Boc-6-aminohexanoic acid |
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Synonym | More Synonyms |
Description | Boc-6-aminohexanoic acid is an alkyl/ether-based PROTAC linker that can be used in the synthesis of PROTACs[1]. |
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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 |
Density | 1.1±0.1 g/cm3 |
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Boiling Point | 380.3±25.0 °C at 760 mmHg |
Melting Point | 35-40 °C |
Molecular Formula | C11H21NO4 |
Molecular Weight | 231.289 |
Flash Point | 183.8±23.2 °C |
Exact Mass | 231.147064 |
PSA | 75.63000 |
LogP | 1.67 |
Vapour Pressure | 0.0±1.8 mmHg at 25°C |
Index of Refraction | 1.464 |
Storage condition | 2-8°C |
Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
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Hazard Codes | Xi |
Risk Phrases | 36/37/38 |
Safety Phrases | S22-S24/25-S26 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
HS Code | 2924199090 |
Precursor 9 | |
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DownStream 10 | |
HS Code | 2924199090 |
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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% |
The literature on affinity chromatography.
Meth. Enzymol. 34 , 3, (1974)
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Affinity chromatography of carboxypeptidase B.
Meth. Enzymol. 34 , 411, (1974)
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Synthesis and properties of radioiodinated phospholipid analogues that spontaneously undergo vesicle-vesicle and vesicle-cell transfer.
Biochemistry 22 , 3617, (1983) An efficient method for the synthesis and purification of a variety of iodinated phospholipid analogues is described. 1-Acyl-2-[[[3-(3-[125I]iodo-4-hydroxyphenyl)- propionyl]amino]caproyl]phosphatidyl... |
6-({[(2-Methyl-2-propanyl)oxy]carbonyl}amino)hexanoic acid |
6-[(2-methylpropan-2-yl)oxycarbonylamino]hexanoic acid |
6-[(tert-butoxycarbonyl)amino]hexanoic acid |
Hexanoic acid, 6-[[(1,1-dimethylethoxy)carbonyl]amino]- |
MFCD00037798 |
Boc-ε-Acp-OH |
Boc-ε-Ahx-OH |