107794
2-硝基苄溴
98%
别名:
α-溴-2-硝基甲苯
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关于此项目
线性分子式:
O2NC6H4CH2Br
化学文摘社编号:
分子量:
216.03
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
223-558-9
Beilstein/REAXYS Number:
638991
MDL number:
产品名称
2-硝基苄溴, 98%
InChI key
HXBMIQJOSHZCFX-UHFFFAOYSA-N
InChI
1S/C7H6BrNO2/c8-5-6-3-1-2-4-7(6)9(10)11/h1-4H,5H2
SMILES string
[O-][N+](=O)c1ccccc1CBr
assay
98%
form
solid
mp
44-46 °C (lit.)
functional group
bromo
nitro
Quality Level
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Application
2-硝基苄基溴用于笼罩水溶液中未保护的含半胱氨酸或硫代磷酸化的肽。其可用于合成（R）-和（S）-3-氨基-3,4-二氢-1 H-喹啉-2-酮。
Biochem/physiol Actions
2-硝基苄基溴与L-半胱氨酸反应生成S-2-硝基苄基半胱氨酸，用于修饰超低温交联琼脂糖。
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
230.0 °F - closed cup
flash_point_c
110 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Kyoung-Ho Park et al.
International journal of molecular sciences, 20(16) (2019-08-21)
A kinetic study was carried out on the solvolysis of o-nitrobenzyl bromide (o-isomer, 1) and p-nitrobenzyl bromide (p-isomer, 3), and o-nitrobenzoyl chloride (o-isomer, 2) in a wide range of solvents under various temperatures. In all of the solvents without aqueous
P Pan et al.
FEBS letters, 405(1), 81-85 (1997-03-17)
Photoreleasable molecules are important in studies of various biological phenomena, especially cell signaling. Here we report a generally applicable approach for 'caging' unprotected cysteine-containing or thiophosphorylated peptides in aqueous solution with 2-nitrobenzyl bromides. Photolysis of the caged peptides was achieved
Ying Luo et al.
Nature materials, 3(4), 249-253 (2004-03-23)
Tissue engineering aims to replace, repair or regenerate tissue/organ function, by delivering signalling molecules and cells on a three-dimensional (3D) biomaterials scaffold that supports cell infiltration and tissue organization. To control cell behaviour and ultimately induce structural and functional tissue
Xu Yang et al.
Polymers, 12(4) (2020-04-09)
Photoresponsive polymers have attracted increasing interest for a variety of applications. Here, we report a family of photoresponsive polypeptoid-based copolymer poly(ethylene glycol)-b-poly(N-(S-(o-nitrobenzyl)-thioethyl) glycine)-co-poly(N-(2-phenylethyl) glycine) (PEG-b-PNSN-co-PNPE) synthesized by the controlled ring-opening polymerization (ROP) technique. The key feature of the design is
A practical synthesis of (R)-and (S)-3-amino-3, 4-dihydro-1H-quinolin-2-one.
Hulin B and Lopaze MG.
Tetrahedron Asymmetry, 15(12), 1957-1958 (2004)
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