18165
(R)-(+)-2-溴丙酸
≥98.0% (sum of enantiomers, GC)
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关于此项目
经验公式（希尔记法）:
C3H5BrO2
化学文摘社编号:
分子量:
152.97
UNSPSC Code:
12352101
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1720262
Assay:
≥98.0% (sum of enantiomers, GC)
Form:
liquid
InChI
1S/C3H5BrO2/c1-2(4)3(5)6/h2H,1H3,(H,5,6)/t2-/m1/s1
SMILES string
C[C@@H](Br)C(O)=O
InChI key
MONMFXREYOKQTI-UWTATZPHSA-N
assay
≥98.0% (sum of enantiomers, GC)
form
liquid
optical activity
[α]20/D +26±2°, neat
refractive index
n20/D 1.475
density
1.692 g/mL at 20 °C (lit.)
functional group
bromo, carboxylic acid
storage temp.
2-8°C
Quality Level
Disclaimer
储存时可变为褐色
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
212.0 °F - closed cup
flash_point_c
100 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
新产品
此项目有
Eugénie Grigorian et al.
Frontiers in microbiology, 12, 725997-725997 (2021-10-09)
L-2-halocid dehalogenases (L-2-HADs) have been mainly characterized from terrestrial polluted environments. By contrast, knowledge is still scarce about their role in detoxification of predominant halocarbons in marine environments. Here, phylogenetic analyses showed a wide diversity of homologous L-2-HADs, especially among
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