| Identification | Back Directory | [Name]
1-BOC-1,8-DIAMINOOCTANE | [CAS]
88829-82-7 | [Synonyms]
SKL028
Boc-DAOct
1-Boc-1,8-diaminooctan
1-BOC-1,8-DIAMINOOCTANE
N1-BOC-1,8-DIAMINOOCTANE
N-Boc-octane-1,8-diamine
N1-Boc-octane-1,8-diamine
TERT-BUTYL 8-AMINOOCTYLCARBAMATE
1,8-Diaminooctane, N1-BOC protected
Octane-1,8-diamine, N-BOC protected
tert-Butyl (8-aminooct-1-yl)carbamate
N-t-Butyloxycarbonyl-1,8-diaminooctane
Octane-1,8-diamine, N-BOC protected 95%
1,8-Diaminooctane, N1-BOC protected 95%
N-tert-Butoxycarbonyl-1,8-octanediaMine
Carbamic acid,N-(8-aminooctyl)-, 1,1-dimethylethyl ester
tert-Butyl 8-aminooctylcarbamate
1,8-Diaminooctane N1-boc protected
tert-Butyl (8-aminooct-1-yl)carbamate, 1,8-Diaminooctane, N-BOC protected | [Molecular Formula]
C13H28N2O2 | [MDL Number]
MFCD02094499 | [MOL File]
88829-82-7.mol | [Molecular Weight]
244.37 |
| Chemical Properties | Back Directory | [Boiling point ]
356.3±25.0 °C(Predicted) | [density ]
0.942±0.06 g/cm3(Predicted) | [storage temp. ]
under inert gas (nitrogen or Argon) at 2–8 °C | [solubility ]
Chloroform, Methanol | [form ]
Solid | [pka]
12.94±0.46(Predicted) | [color ]
Off-White | [InChI]
InChI=1S/C13H28N2O2/c1-13(2,3)17-12(16)15-11-9-7-5-4-6-8-10-14/h4-11,14H2,1-3H3,(H,15,16) | [InChIKey]
BEHVGNKIRNVBPF-UHFFFAOYSA-N | [SMILES]
C(OC(C)(C)C)(=O)NCCCCCCCCN |
| Hazard Information | Back Directory | [Description]
tert-butyl (8-aminooctyl)carbamate can be used as a PROTAC linker in the synthesis of PROTACs. tert-butyl (8-aminooctyl)carbamate is an alkane chain with terminal amine and Boc-protected amino groups. Amine group is reactive with carboxylic acids, activated NHS esters, carbonyls (ketone, aldehyde) etc. The Boc group can be deprotected under mild acidic conditions to form the free amine. | [Uses]
tert-Butyl (8-aminooctyl)carbamate (1-Boc-1,8-diaminooctane) can be used as a PROTAC linker in the synthesis of PROTACs. tert-butyl (8-aminooctyl)carbamate is an alkane chain with terminal amine and Boc-protected amino groups. Amine group is reactive with carboxylic acids, activated NHS esters, carbonyls (ketone, aldehyde) etc. The Boc group can be deprotected under mild acidic conditions to form the free amine. |
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| Company Name: |
J & K SCIENTIFIC LTD.
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| Telephone: |
18210857532 18210857532 |
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https://www.jkchemical.com |
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Energy Chemical
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400-0056266 |
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www.energy-chemical.com |
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Jia Xing Isenchem Co.,Ltd
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0573-85285100 18627885956 |
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https://www.chemicalbook.com/ShowSupplierProductsList14265/0_EN.htm |
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T&W GROUP
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skychemical Co.Ltd
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http://www.skychemical.com |
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parabiochem
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025-83453382-8005 |
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www.parabiochem.cn |
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