372404
1,3-二溴-2-丙醇
technical grade, 95%
别名:
α,γ-Dibromohydrin, α-Dibromohydrin, 1,3-Dibromo-2-hydroxypropane, 1,3-Dibromohydrin, 1,3-Dibromopropanol, 2-Hydroxy-1,3-dibromopropane, Glycerol α,γ-dibromohydrin, Glycerol 1,3-dibromohydrin
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关于此项目
线性分子式:
BrCH2CH(OH)CH2Br
化学文摘社编号:
分子量:
217.89
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
202-489-8
MDL number:
产品名称
1,3-二溴-2-丙醇, technical grade, 95%
InChI key
KIHQZLPHVZKELA-UHFFFAOYSA-N
InChI
1S/C3H6Br2O/c4-1-3(6)2-5/h3,6H,1-2H2
SMILES string
OC(CBr)CBr
grade
technical grade
assay
95%
form
liquid
refractive index
n20/D 1.552 (lit.)
bp
82-83 °C/7 mmHg (lit.)
density
2.136 g/mL at 25 °C (lit.)
functional group
bromo
hydroxyl
Quality Level
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Application
1,3-Dibromo-2-propanol may be used in the following studies:
- To prepare the thioether ligand, used in the synthesis of palladium-phosphorus/sulfur nanoparticles.
- Preparation of 2-(alkoxy)propenyl bromide.
- Synthesis of 1,3-propanediamine derivatives connected to carbohydrates (sugar-pendant diamines).
- Chemical crosslinking of nine single substitution cysteine mutants of staphylococcal nuclease.
- Preparation of 1,3-dinitrooxy-2-propanol, via reaction with AgNO3 in MeCN at 80°C.
General description
1,3-Dibromo-2-propanol is a dihalogenated alcohol. It is reported as bifunctional crosslinking reagent.
signalword
Danger
Hazard Classifications
Acute Tox. 3 Oral - Carc. 2 - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
3 - Flammable liquids
wgk
WGK 3
flash_point_f
116.6 °F - closed cup
flash_point_c
47 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
M P Byrne et al.
Protein science : a publication of the Protein Society, 4(12), 2545-2558 (1995-12-01)
Nine single substitution cysteine mutants of staphylococcal nuclease (nuclease) were preferentially crosslinked at the introduced cysteine residues using three different bifunctional crosslinking reagents; 1,6-bismaleimidohexane (BMH), 1,3-dibromo-2-propanol (DBP), and the chemical warfare agent, mustard gas (bis(2-chloroethyl)sulfide; mustard). BMH and mustard gas
Rudong Shan et al.
Journal of medicinal chemistry, 47(1), 254-261 (2003-12-30)
A novel group of hybrid calcium channel (CC) modulators was prepared where the isopropyl ester moiety of isopropyl 1,4-dihydro-2,6-dimethyl-3-nitro-4-(2,1,3-benzoxadiazol-4-yl)pyridine-5-carboxylate (PN 202-791) was replaced by a variety of nitric oxide (*NO) donor nitrooxyalkyl ester substituents. Enantiomers, or diastereomers, having the (R)-configuration
Hemant Joshi et al.
Nanoscale, 6(9), 4588-4597 (2014-03-15)
PdP2 and Pd4S nanoparticles (NPs) (size: ∼2-6 and 9-15 nm respectively) have been prepared for the first time from a single source precursor complex [Pd(L)Cl2] (1) by its one pot thermolysis at 200 °C in TOP and OA/ODE (1 : 1) respectively.
Daisuke Kugimoto et al.
Polymers, 13(3) (2021-02-13)
Associating behavior of star-like amphiphilic polymers consisting of two or three poly(ethylene oxide) (PEO) chains and one stearyl chain (C18) was investigated. Although the aggregation number (Nagg) of linear analogue of amphiphilic polymers monotonically decreased with increasing number-average molecular weight
Y Mikata et al.
The Journal of organic chemistry, 66(11), 3783-3789 (2001-05-26)
A set of 1,3-propanediamine derivatives connected to carbohydrates (5) has been prepared in four steps from peracetylated sugar and 1,3-dibromo-2-propanol in 60-73% yields. D-Glucose, D-mannose, D-galactose, D-xylose, D-ribose, and maltose are utilized as sugar molecules in this work. The diamine
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