142514
3-Bromopropionyl chloride
technical grade
Synonym(s):
β-Bromopropanoyl chloride, β-Bromopropionyl chloride, ψ-Bromopropanoyl chloride, 3-Bromopropanoic acid chloride, 3-Bromopropanoyl chloride
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About This Item
Linear Formula:
BrCH2CH2COCl
CAS Number:
Molecular Weight:
171.42
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
239-515-2
MDL number:
Form:
liquid
grade
technical grade
Quality Level
form
liquid
refractive index
n20/D 1.49 (lit.)
bp
55-57 °C/17 mmHg (lit.)
density
1.701 g/mL at 25 °C (lit.)
functional group
acyl chloride, bromo
storage temp.
2-8°C
SMILES string
ClC(=O)CCBr
InChI
1S/C3H4BrClO/c4-2-1-3(5)6/h1-2H2
InChI key
IHBVNSPHKMCPST-UHFFFAOYSA-N
General description
3-Bromopropionyl chloride reacts with poly(ethylene glycol) methacrylate to yield brominated poly(ethylene glycol) methacrylate. It causes the acylation of 4-aryl-substituted 3,4-di-hydropyrimidine(1H)-2-thiones to give bicyclic pyrimido[2,1-b][1,3]thiazines.
Application
3-Bromopropionyl chloride was used in the preparation of 1-chloro-4-bromo-2-butanone.
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B - STOT SE 3
target_organs
Respiratory system
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
174.2 °F - closed cup
flash_point_c
79 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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Synthesis and Characterization of a Novel Macromonomer Initiator for Reversible Addition Fragmentation Chain Transfer (RAFT). Evaluation of the Polymerization Kinetics and Gelation Behaviors.
Ozturk T and Hazer B.
Journal of Macromolecular Science, Part A: Pure and Applied Chemistry, 47(3), 265-272 (2010)
Synthesis of bicyclic pyrimido [2, 1-b][1, 3] thiazines based on 3, 4-dihydropyrimidine-(1H)-2-thiones.
Kulakov IV and Turdybekov DM.
Chemistry of Heterocyclic Compounds, 46(3), 342-346 (2010)
A Nagy et al.
Proceedings of the National Academy of Sciences of the United States of America, 93(6), 2464-2469 (1996-03-19)
A convenient, high yield conversion of doxorubicin to 3'-deamino-3'-(2''-pyrroline-1''-yl)doxorubicin is described. This daunosamine-modified analog of doxorubicin is 500-1000 times more active in vitro than doxorubicin. The conversion is effected by using a 30-fold excess of 4-iodobutyraldehyde in anhydrous dimethylformamide. The
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 142514-100G | 04061836682361 |
| 142514-25G | 04061838734372 |