Skip to Content
Merck
CN

142514

3-Bromopropionyl chloride

technical grade

Synonym(s):

β-Bromopropanoyl chloride, β-Bromopropionyl chloride, ψ-Bromopropanoyl chloride, 3-Bromopropanoic acid chloride, 3-Bromopropanoyl chloride

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Linear Formula:
BrCH2CH2COCl
CAS Number:
15486-96-1
Molecular Weight:
171.42
NACRES:
NA.22
PubChem Substance ID:
24848528
UNSPSC Code:
12352100
EC Number:
239-515-2
MDL number:
MFCD00000746

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

3-Bromopropionyl chloride, technical grade

InChI key

IHBVNSPHKMCPST-UHFFFAOYSA-N

InChI

1S/C3H4BrClO/c4-2-1-3(5)6/h1-2H2

SMILES string

ClC(=O)CCBr

grade

technical grade

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

Quality Level

100

Related Categories

Application

3-Bromopropionyl chloride was used in the preparation of 1-chloro-4-bromo-2-butanone.

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.

pictograms

CorrosionExclamation mark
GHS05,GHS07

signalword

Danger

hcodes

H314,H335

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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
MKCV1864
MKCR4028
MKCM4339
MKCK9676
MKCH6928

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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
Ji Eon Chae et al.
Polymers, 13(5) (2021-03-07)
Polystyrene-based polymers with variable molecular weights are prepared by radical polymerization of styrene. Polystyrene is grafted with bromo-alkyl chains of different lengths through Friedel-Crafts acylation and quaternized to afford a series of hydroxide-ion-conducting ionomers for the catalyst binder for the

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service