N-Boc-ethylenediamine - CAS 57260-73-8
Catalog: |
BB029620 |
Product Name: |
N-Boc-ethylenediamine |
CAS: |
57260-73-8 |
Synonyms: |
tert-butyl N-(2-aminoethyl)carbamate |
IUPAC Name: | tert-butyl N-(2-aminoethyl)carbamate |
Description: | NH2-C2-NH-Boc is a PROTAC linker, which refers to the alkyl chain composition. NH2-C2-NH-Boc can be used in the synthesis of a series of PROTACs. |
Molecular Weight: | 160.21 |
Molecular Formula: | C7H16N2O2 |
Canonical SMILES: | CC(C)(C)OC(=O)NCCN |
InChI: | InChI=1S/C7H16N2O2/c1-7(2,3)11-6(10)9-5-4-8/h4-5,8H2,1-3H3,(H,9,10) |
InChI Key: | AOCSUUGBCMTKJH-UHFFFAOYSA-N |
Boiling Point: | 80-84 ℃ (0.3 mmHg) |
Density: | 1.016 g/cm3 |
Solubility: | 10 mM in DMSO |
Storage: | 4 ℃, protect from light *In solvent : -80 ℃, 6 months; -20 ℃, 1 month (protect from light) |
MDL: | MFCD00191871 |
LogP: | 1.56100 |
GHS Hazard Statement: | H314 (98.08%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation] |
Precautionary Statement: | P260, P264, P280, P301+P330+P331, P303+P361+P353, P304+P340, P305+P351+P338, P310, P321, P363, P405, and P501 |
Signal Word: | Danger |
Publication Number | Title | Priority Date |
CN-113354619-A | Compound for targeted ubiquitination degradation of tyrosinase and preparation method and application thereof | 20210624 |
CN-112979532-A | Phthalimide compound, preparation method and application | 20210520 |
CN-112979532-B | Phthalimide compound, preparation method and application | 20210520 |
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PMID | Publication Date | Title | Journal |
22679528 | 20120101 | (α,α-dimethyl)glycyl (dmg) PNAs: achiral PNA analogs that form stronger hybrids with cDNA relative to isosequential RNA | Artificial DNA, PNA & XNA |
20427036 | 20100616 | Synthesis of a C-galactopyranosyl-linked N-substituted 1,2-ethylenediamine | Carbohydrate research |
18543915 | 20080709 | Approach to formation of multifunctional polyester particles in controlled nanoscopic dimensions | Journal of the American Chemical Society |
18314939 | 20080301 | Novel biodegradable poly(disulfide amine)s for gene delivery with high efficiency and low cytotoxicity | Bioconjugate chemistry |
18205157 | 20080101 | Covalent tethering of organic functionality to the surface of glassy carbon electrodes by using electrochemical and solid-phase synthesis methodologies | Chemistry (Weinheim an der Bergstrasse, Germany) |
Complexity: | 129 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 160.121177757 |
Formal Charge: | 0 |
Heavy Atom Count: | 11 |
Hydrogen Bond Acceptor Count: | 3 |
Hydrogen Bond Donor Count: | 2 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 160.121177757 |
Rotatable Bond Count: | 4 |
Topological Polar Surface Area: | 64.4 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 0 |
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