Interesting facts
Interesting Facts about 2-(2-Aminoethyl)isothiourea Dihydrobromide
2-(2-Aminoethyl)isothiourea dihydrobromide is a fascinating chemical compound renowned in the fields of biochemistry and medicinal chemistry. Here are some noteworthy aspects of this compound:
- Versatile Reactivity: This compound features functional groups that allow it to participate in a variety of chemical reactions, making it a useful intermediate in organic synthesis.
- Biological Activity: It possesses potential biological applications, particularly as an inhibitor of certain enzymes, which makes it a candidate for drug discovery and development.
- Research Significance: “A compound that bridges the gap between synthetic chemistry and biological applications” is how many researchers describe it. Its ability to mimic certain amino acids enhances its relevance in biological studies.
- Analytical Applications: Due to its unique structure, it can be used in various analytical techniques including chromatography and mass spectrometry, which aids in understanding complex biochemical pathways.
- Synthesis Challenges: The synthesis of 2-(2-aminoethyl)isothiourea dihydrobromide is quite detailed and requires careful control of reaction conditions to obtain optimal yield, showcasing the intricate dance of organic chemistry.
Overall, 2-(2-aminoethyl)isothiourea dihydrobromide represents an intriguing area of study for chemists and biochemists alike, bridging the gap between synthetic methodology and practical applications in health sciences.
Synonyms
56-10-0
2-(2-Aminoethyl)isothiourea dihydrobromide
Antiradon
2-aminoethyl carbamimidothioate dihydrobromide
Antirad
Ixecur
aet
2-(2-Aminoethyl)-2-thiopseudourea dihydrobromide
Carbamimidothioic acid, 2-aminoethyl ester, dihydrobromide
S-2-Aminoethylthiouronium bromide hydrobromide
USAF XR-31
AE-ITU (dihydrobromide)
MFCD00037011
beta-Aminoethylisothiouronium bromide hydrobromide
S-(2-Aminoethyl)-ITU dihydrobromide
03K18418PY
S-(2-Aminoethyl)isothiuronium bromide hydrobromide
beta-Aminoethyl isothiourea
Carbamimidothioic acid, 2-aminoethyl ester, hydrobromide (1:2)
Aminoethylisothiuronium bromide hydrobromide
NSC-22877
S-Aminoethylisothiuronium bromide hydrobromide
2-(2-Aminoethyl)-2-thiopseudourea hydrobromide
AMINOETHYLISOTHIOUREA DIHYDROBROMIDE
A 15591
A. E. T.
S-(2-Aminoethyl)isothiouronium bromide hydrobromide
.beta.-Aminoethylisothiuronium bromide hydrobromide
[(2-aminoethyl)sulfanyl]methanimidamide dihydrobromide
S-(2-Aminoethyl)Isothiourea Dihydrobromide
DTXSID1058765
SR-01000075171
2-Aminoethylisothiouronium dibromide
EINECS 200-257-0
NSC 22877
2-Aminoethylisothiuronium dihydrobromide
S-(2-Aminoethyl)isothiuronium dibromide
2-Aminoethylthiopseudourea dihydrobromide
S-beta-Aminoethylisothiuronium bromohydrate
AI3-23427
S-(2-Aminoethyl)pseudothiourea dihydrobromide
UNII-03K18418PY
2-Aminoethylisothiuronium bromide hydrobromide
Isothiuronium bromide, aminoethyl-, hydrobromide
S-(2-Aminoaethyl)isothiuronium dibromid [German]
S-2-Aminoethylisothiouronium bromide hydrobromide
beta-Aminoethylisothiuronium Bromide
2beta-Aminoethylisothiourea-bromide-hydrogen bromide
Pseudourea, (2-aminoethyl)-2-thio-, dihydrobromide
beta-Aminoaethyl-isothiuronium dihydrobromid [German]
2-(beta-Aminoethyl)isothiouronium bromide hydrobromide
S-(2-Aminoaethyl)isothiuronium dibromid
beta-Aminoaethyl-isothiuronium dihydrobromid
2-aminoethyl carbamimidothioate;dihydrobromide
AET [MI]
927-71-9
SPECTRUM1505119
2-AMINOETHYLSULFANYLMETHANIMIDAMIDE DIHYDROBROMIDE
CHEMBL1256182
DTXCID2042012
XDVMCVGTDUKDHL-UHFFFAOYSA-N
AMBINTER LT03383002
2-(2-Aminoethyl)isothiourea diHBr
STR04872
Tox21_500078
AKOS015962093
CCG-214521
LP00078
NCGC00093585-01
NCGC00093585-02
NCGC00260763-01
2-(2-Aminoethyl)isothioureadihydrobromide
AC-15654
PD000618
HY-131929
S-(2-aminoethyl)isothiourea di-hydrobromide
CS-0143720
EU-0100078
A 5879
D88373
EN300-6963435
2-(2-Aminoethyl)isothiourea dihydrobromide, 99%
AET; S-(2-Aminoethyl)isothiouronium dihydrobromide
SR-01000075171-1
SR-01000075171-3
SR-01000075171-7
Q27247570
BETA-AMINOETHYLISOTHIURONIUM BROMIDE HYDROBROMIDE
Solubility of 2-(2-aminoethyl)isothiourea;dihydrobromide
The compound 2-(2-aminoethyl)isothiourea;dihydrobromide (C3H10N2S · 2 HBr) exhibits notable solubility characteristics that are worth highlighting:
As with many nitrogen-containing compounds, care should be taken when interpreting solubility data, as various factors can lead to increased or decreased solubility. Understanding these parameters can be crucial for applications in biochemical contexts where solubility plays a vital role in bioavailability and reaction kinetics.