2-Thiazolamine, 5-bromo-

5-BROMO-THIAZOL-2-YLAMINE · 5-broMo-1,3-thiazol-2-aMine · 5-broMo-2-aMino-thiazole · 5-BROMO-2-AMINOTHIAZOLE HYDROBROMIDE · TIMTEC-BB SBB000204 · 5-Bromo-2-thiazolamine · 2-AMINO-5-BROMOTHIAZOLE · 5-Bromothiazole-2-amine

https://huagongshe.com/de/chemical/43600

Molekülstruktur von 2-Thiazolamine, 5-bromo-

Identifikatoren & physikalische Daten

CAS No.	3034-22-8
Summenformel	C3H3BrN2S
Durchschnittliche Molmasse	179,04 g/mol
Monoisotopische Masse	177,9200312 g/mol
SMILES	Nc1ncc(Br)s1
InChIKey	ARHCLXWELPFVFQ-UHFFFAOYSA-N
PubChem CID	43600
ChEMBL	CHEMBL5179176
EC No.	819-500-2
DTXSID	DTXSID20275455

Chemische & physikalische Eigenschaften

XLogP	1,7
Polarare Oberfläche (TPSA)	67,2
H-Brücken-Donoren	1
H-Brücken-Akzeptoren	3
Frei drehbare Bindungen	0
Schwere Atome	7
Formalladung	0
Komplexität	70
Schmelzpunkt	165 °C (dec.)(lit.)
Siedepunkt	287.6±13.0 °C(Predicted)
Dichte	1.976±0.06 g/cm3(Predicted)
Lagerbedingungen	Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
Aggregatzustand	solid
pKa (Säurekonstante)	3.22±0.10(Predicted)
Farbe	White
InChI	InChI=1S/C3H3BrN2S/c4-2-1-6-3(5)7-2/h1H,(H2,5,6)
InChIKey	ARHCLXWELPFVFQ-UHFFFAOYSA-N
SMILES	S1C(Br)=CN=C1N
CAS Datenbank	3034-22-8(CAS DataBase Reference)

Sicherheit & Vorschriften

GHS-Einstufung	WarningH315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)The GHS information provided by 1 company from 1 notification to the ECHA C&L Inventory.
Regulatorische Informationen	2-Thiazolamine, 5-bromo-: Does not have an individual approval but may be used under an appropriate group standard
Hazard Classes and Categories	Skin Irrit. 2 (100%)
Zollcode	2934100090
RTECS-Nr.	XJ1262200
R-Sätze (R)	22-36
Gefahrensymbole	Xn
Sicherheitshinweise (S)	26-36/37

Anwendungen & Verwendung

Verwenden

2-Amino-5-bromothiazole is a type of aliphatic hydrocarbon that has been synthesized by Friedel-Crafts acylation. This chemical is used to neutralize typhimurium and can be used in the synthesis of other compounds. The functional theory on how 2-amino-5-bromothiazole works may be due to its ability to form nitro groups, which are highly reactive and cause depression in the reaction scheme. 2-Amino-5-bromothiazole is often used as a test organism for other organisms in order to measure their sensitivity to different types of chemicals. It has also been shown that it has an effect on hydrocarbons, which have been shown to have an effect on organisms such as bacteria.