128023
2-氨基-5-溴噻唑 单氢溴酸盐
97%
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关于此项目
经验公式（希尔记法）:
C3H3BrN2S · HBr
化学文摘社编号:
分子量:
259.95
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
262-699-0
MDL number:
Assay:
97%
Form:
solid
InChI key
NUSVDASTCPBUIP-UHFFFAOYSA-N
InChI
1S/C3H3BrN2S.BrH/c4-2-1-6-3(5)7-2;/h1H,(H2,5,6);1H
SMILES string
Br[H].Nc1ncc(Br)s1
assay
97%
form
solid
mp
165 °C (dec.) (lit.)
functional group
bromo
Application
2-Amino-5-bromothiazole monohydrobromide was used in the preparation of N-(5-Bromo-2-thiazolyl)-2-acetylamino-2-ethoxycarbonyl-3-(2-furyl)-propanamide.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
T Kitagawa et al.
Chemical & pharmaceutical bulletin, 49(3), 335-339 (2001-03-20)
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 was prepared via condensation of 2-(bromomethyl)furan (10b) with diethyl acetamidomalonate, followed by partial hydrolysis of the resultant diethyl ester (3a) in the presence of
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