372404
1,3-Dibromo-2-propanol
technical grade, 95%
동의어(들):
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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5 G
₩59,885
25 G
₩197,012
About This Item
Linear Formula:
BrCH2CH(OH)CH2Br
CAS Number:
Molecular Weight:
217.89
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22
추천 제품
Grade
technical grade
Quality Level
분석
95%
양식
liquid
refractive index
n20/D 1.552 (lit.)
bp
82-83 °C/7 mmHg (lit.)
density
2.136 g/mL at 25 °C (lit.)
작용기
bromo
hydroxyl
SMILES string
OC(CBr)CBr
InChI
1S/C3H6Br2O/c4-1-3(6)2-5/h3,6H,1-2H2
InChI key
KIHQZLPHVZKELA-UHFFFAOYSA-N
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일반 설명
1,3-Dibromo-2-propanol is a dihalogenated alcohol. It is reported as bifunctional crosslinking reagent.[1]
애플리케이션
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.[2]
- Preparation of 2-(alkoxy)propenyl bromide.[3]
- Synthesis of 1,3-propanediamine derivatives connected to carbohydrates (sugar-pendant diamines).[4]
- Chemical crosslinking of nine single substitution cysteine mutants of staphylococcal nuclease.[1]
- Preparation of 1,3-dinitrooxy-2-propanol, via reaction with AgNO3 in MeCN at 80°C.[5]
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 3 Oral - Carc. 2 - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point (°F)
116.6 °F - closed cup
Flash Point (°C)
47 °C - closed cup
개인 보호 장비
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
이미 열람한 고객
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
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
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.
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
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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