150452
6-溴己酸
97%
别名:
6-溴代己酸
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关于此项目
线性分子式:
BrCH2(CH2)4COOH
化学文摘社编号:
分子量:
195.05
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
224-176-5
Beilstein/REAXYS Number:
1749740
MDL number:
产品名称
6-溴己酸, 97%
InChI key
NVRVNSHHLPQGCU-UHFFFAOYSA-N
InChI
1S/C6H11BrO2/c7-5-3-1-2-4-6(8)9/h1-5H2,(H,8,9)
SMILES string
OC(=O)CCCCCBr
assay
97%
form
solid
bp
165-170 °C/20 mmHg (lit.)
mp
32-34 °C (lit.)
functional group
bromo
carboxylic acid
Quality Level
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Application
6-溴己酸被用于在使用甲苯磺酰异氰酸酯（189278）处理时制备N-酰基磺酰胺，以及从烷基碘和金属锶制备烷基酮。它还用于合成阴离子丝裂霉素C-葡聚糖偶联物（MMC-D）、2-锂-1,3-二噻烷和二芳基硫醚。
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
203.0 °F - closed cup
flash_point_c
95 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Vinzenz Bachler
Journal of computational chemistry, 28(12), 2013-2019 (2007-04-05)
Localized bonding schemes and their weights have been obtained for the pi-electron system of nitrone by expanding complete active space self-consistent field wave functions into a set of Slater determinants composed of orthogonal natural atomic orbitals (NAOs) of Weinhold and
Tetrahedron Letters, 48, 787-787 (2007)
S S Pochapsky et al.
Bioconjugate chemistry, 1(4), 231-244 (1990-07-01)
A versatile method for the synthesis of trifluoro fatty acids, potential metabolically blocked myocardial imaging agents, has been developed. Two trifluorohexadecanoic (palmitic) acids have been prepared [6,6,16-trifluorohexadecanoic acid (I) and 7,7,16-trifluorohexadecanoic acid (II)], each of which bears two of the
D Poirier et al.
Journal of medicinal chemistry, 37(8), 1115-1125 (1994-04-15)
The reaction of 1,2-diarylethanol and mercapto side chain catalyzed by ZnI2 was used as a key step in the short (three to five steps) and efficient synthesis of 17 diaryl thioether derivatives. Several of these compounds contain a methyl butyl
S Matsumoto et al.
Cancer research, 46(9), 4463-4468 (1986-09-01)
Cellular interaction and in vitro antitumor activity of a polymeric prodrug of mitomycin C (MMC), mitomycin C-dextran conjugate (MMC-D), were studied in relation to its physicochemical characteristics. MMC-D with cationic and anionic charges were examined. The cationic MMC-D was synthesized
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