2-Amino-5-bromothiazole hydrobromide
Suppliers
Names
[ CAS No. ]:
61296-22-8
[ Name ]:
2-Amino-5-bromothiazole hydrobromide
[Synonym ]:
2-Amino-5-bromothiazole monohydrobromide
2-Thiazolamine, 5-bromo-, hydrobromide (1:1)
5-bromo-1,3-thiazol-2-amine,hydrobromide
MFCD00012712
2-Amino-5-bromothiazole hydrobromide
5-Bromo-1,3-thiazol-2-amine hydrobromide (1:1)
5-Bromo-1,3-thiazol-2-amine hydrobromide
EINECS 262-699-0
Chemical & Physical Properties
[ Boiling Point ]:
192.5ºC at 760 mmHg
[ Melting Point ]:
165 °C (dec.)(lit.)
[ Molecular Formula ]:
C3H4Br2N2S
[ Molecular Weight ]:
259.95
[ Flash Point ]:
70.2ºC
[ Exact Mass ]:
257.846191
[ PSA ]:
67.15000
[ LogP ]:
3.02710
MSDS
Toxicological Information
CHEMICAL IDENTIFICATION
- RTECS NUMBER :
- XJ1262200
- CHEMICAL NAME :
- 2-Thiazolamine, 5-bromo-, monohydrobromide
- CAS REGISTRY NUMBER :
- 61296-22-8
- LAST UPDATED :
- 199410
- DATA ITEMS CITED :
- 2
- MOLECULAR FORMULA :
- C3-H3-Br-N2-S.Br-H
- MOLECULAR WEIGHT :
- 259.97
HEALTH HAZARD DATA
ACUTE TOXICITY DATA
MUTATION DATA
- TYPE OF TEST :
- Mutation in microorganisms
- TEST SYSTEM :
- Bacteria - Klebsiella pneumoniae
- DOSE/DURATION :
- 200 umol/L
- REFERENCE :
- MUREAV Mutation Research. (Elsevier Science Pub. B.V., POB 211, 1000 AE Amsterdam, Netherlands) V.1- 1964- Volume(issue)/page/year: 118,153,1983
Safety Information
[ Symbol ]:
GHS07
[ Signal Word ]:
Warning
[ Hazard Statements ]:
H302-H319
[ Precautionary Statements ]:
P305 + P351 + P338
[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves
[ Hazard Codes ]:
Xn: Harmful;
[ Risk Phrases ]:
R22
[ Safety Phrases ]:
S26-S36/37-S24/25
[ RIDADR ]:
NONH for all modes of transport
[ RTECS ]:
XJ1262200
[ HS Code ]:
2934100090
Precursor & DownStream
Precursor
DownStream
Customs
[ HS Code ]: 2934100090
[ Summary ]:
2934100090 other compounds containing an unfused thiazole ring (whether or not hydrogenated) in the structure VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:20.0%
Articles
Chem. Pharm. Bull. 49(3) , 335-339, (2001)
N-Substituted 2-acetylamino-2-ethoxycarbonyl-3-(2-furyl)propanamides (8) were synthesized through the reaction of amines (13) with 2-acetylamino-2-ethoxycarbonyl-3-(2-furyl)propanoic acid (3b), which ...