249785
2-Bromopropionyl bromide
97%
Sinónimos:
α-Bromopropanyl bromide, α-Bromopropionyl bromide, (±)-2-Bromopropanoyl bromide, 2-Bromopropanoyl bromide
Iniciar sesión para ver los precios por organización y contrato.
Seleccione un Tamaño
Cambiar Vistas
Acerca de este artículo
Fórmula lineal:
CH3CHBrCOBr
Número CAS:
Peso molecular:
215.87
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
209-261-7
Beilstein/REAXYS Number:
1071331
MDL number:
Assay:
97%
Form:
liquid
Servicio técnico
¿Necesita ayuda? Nuestro equipo de científicos experimentados está aquí para ayudarle.
Permítanos ayudarlevapor density
7.5 (vs air)
Quality Level
vapor pressure
1.3 mmHg ( 20 °C)
assay
97%
form
liquid
refractive index
n20/D 1.518 (lit.)
bp
48-50 °C/10 mmHg (lit.)
density
2.061 g/mL at 25 °C (lit.)
functional group
acyl bromide, bromo
SMILES string
CC(Br)C(Br)=O
InChI
1S/C3H4Br2O/c1-2(4)3(5)6/h2H,1H3
InChI key
ILLHORFDXDLILE-UHFFFAOYSA-N
Application
2-Bromopropionyl bromide has been used in the synthesis of:
- cellulose macroinitiator via direct acylation of cellulose in ionic liquid 1-allyl-3-methylimidazolium chloride
- 3-(2-bromopropionyl)-2-oxazolidone derivatives
- bromoester terminated poly(3-hexylthiophene), used as macroinitiator for atom transfer radical polymerization of acrylates.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Skin Corr. 1B
Clase de almacenamiento
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Elija entre una de las versiones más recientes:
¿Ya tiene este producto?
Encuentre la documentación para los productos que ha comprado recientemente en la Biblioteca de documentos.
A highly stereoselective synthesis of a key intermediate of 1?-methylcarbapenems employing the reformatsky reaction of 3-(2-bromopropionyl)-2-oxazolidone derivatives.
Ito Y and Terashima S.
Tetrahedron Letters, 28(52), 6625-6628 (1987)
Xiaofeng Sui et al.
Biomacromolecules, 9(10), 2615-2620 (2008-09-09)
Cellulose-graft-poly(N,N-dimethylamino-2-ethyl methacrylate) (cellulose-g-PDMAEMA) copolymers were prepared by homogeneous atom transfer radical polymerization (ATRP) under mild conditions. Cellulose macroinitiator was successfully synthesized by direct acylation of cellulose with 2-bromopropionyl bromide in a room temperature ionic liquid (RTIL), 1-allyl-3-methylimidazolium chloride. Copolymers were
Regioregular poly (3-alkylthiophene) conducting block copolymers.
Iovu MC, et al.
Polymer, 46(19), 8582-8586 (2005)