ChemicalBook > CAS DataBase List > 3-Chloropropionyl chloride

3-Chloropropionyl chloride

Product Name
3-Chloropropionyl chloride
CAS No.
625-36-5
Chemical Name
3-Chloropropionyl chloride
Synonyms
3-Chloropropanoyl chloride;Chloropropionyl chloride;oropropionyL;3-Chloropropionyl ch;3-Chlorpropionylchlorid;-Chloropropanoylchloride;3-Chloropropinyl chloride;3-chloro-propanoylchlorid;3-CHLOROPROPIONYL CHLORIDE;3-Chloropropionyl chlorode
CBNumber
CB8691211
Molecular Formula
C3H4Cl2O
Formula Weight
126.97
MOL File
625-36-5.mol
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3-Chloropropionyl chloride Property

Melting point:
-32 °C
Boiling point:
143-145 °C(lit.)
Density 
1.33 g/mL at 25 °C(lit.)
vapor pressure 
10.0 hPa
refractive index 
n20/D 1.457(lit.)
RTECS 
UC3934000
Flash point:
146 °F
storage temp. 
Flammables area
solubility 
Chloroform, Ethyl Acetate
form 
liquid
color 
red-brown
PH
<7 (H2O)
explosive limit
8.8-20.2%(V)
Water Solubility 
reacts
Sensitive 
Moisture Sensitive
BRN 
635814
Stability:
Moisture Sensitive
InChIKey
INUNLMUAPJVRME-UHFFFAOYSA-N
CAS DataBase Reference
625-36-5(CAS DataBase Reference)
NIST Chemistry Reference
Propanoyl chloride, 3-chloro-(625-36-5)
EPA Substance Registry System
Propanoyl chloride, 3-chloro- (625-36-5)
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Safety

Hazard Codes 
T+
Risk Statements 
14-22-26-34-35-10
Safety Statements 
23-26-36/37/39-45-38-16-8
RIDADR 
UN 3390 6.1/PG 1
WGK Germany 
1
21
TSCA 
Yes
HazardClass 
6.1
PackingGroup 
I
HS Code 
29159080
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H302Harmful if swallowed

H314Causes severe skin burns and eye damage

H330Fatal if inhaled

Precautionary statements

P260Do not breathe dust/fume/gas/mist/vapours/spray.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

P303+P361+P353IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
C69128
Product name
3-Chloropropionyl chloride
Purity
98%
Packaging
100g
Price
$137
Updated
2024/03/01
Sigma-Aldrich
Product number
147443
Product name
3-Chloropropionyl chloride
Purity
technical grade
Packaging
100ml
Price
$56.4
Updated
2024/03/01
Alfa Aesar
Product number
B25698
Product name
3-Chloropropionyl chloride, 97%
Packaging
100g
Price
$78.8
Updated
2024/03/01
TRC
Product number
C380600
Product name
3-Chloropropionyl chloride
Packaging
5g
Price
$45
Updated
2021/12/16
Biosynth Carbosynth
Product number
FC71810
Product name
3-Chloropropionyl chloride
Packaging
50g
Price
$50
Updated
2021/12/16
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3-Chloropropionyl chloride Chemical Properties,Usage,Production

Description

3-Chloropropionyl chloride is an important bifunctional reagent. It is capable of acylation and possesses a 2-chloro-ethyl fragment (CH2CH2Cl), which can be subjected to nucleophilic substitution and serves as a masked vinyl group. It can be used as a starting material in many reactions to construct a variety of (hetero)cyclic compounds.

Chemical Properties

Clear colorless to dark brown liquid. Soluble in ethanol, ether and chloroform. Slightly soluble in water.

Uses

3-Chloropropionyl chloride is a reagent used in the synthesis of Beclamide (B119400), which is a chlorinated benzylpropanamide used as an anticonvulsant drug. It is used in the treatment of tonic-clonic seizyres and has sedative properties.

Preparation

3-Chloropropionyl chloride (1) is commercially available and can be prepared from β-propiolactone (2) and thionyl chloride.1 Other standard methods available for the preparation of acyl chlorides can also be applied: the reaction of acrylic acid (3) or 3-chloropropionic acid (4) with thionyl chloride, phosphoryl chloride, phosgene, or phosphorus trichloride.

Reactions

(1) The Friedel¨CCrafts acylation of tert-butylbenzene (5) with 3-chloropropionyl chloride (1) followed by cyclization provid- ed indanone 6, which was further transformed into urea derivative 7, a potent TRPV1 antagonist.

(2) A novel high-yielding one-pot microwave-assisted synthesis of condensed 5-substituted pyranoisoquinoline-1,6-diones 9 from 2-substituted isoquinoline-1,3-diones 8 and 3-chloropropionyl chloride (1) was reported.

(3) Acylation of 2-aminophenol (12) with 3-chloropropionyl chloride (1), followed by cyclization in the presence of polyphosphoric acid (PPA), gave benzoxazole 13, which was further reacted with 4-chlorophenyl-1-piperazine to yield the target benzo[d]oxazole analogue 14, a selective dopamine D4 receptor ligand.

Flammability and Explosibility

Non flammable

Synthesis

3-Chloropropionyl chloride is produced by reaction of acrylic acid with hydrogen chloride and phosgene in the presence of, for example,dimethylformamide as catalyst, or by reaction of propiolactone with thionyl chloride.

Synthesis

3-Chloropropionyl chloride is produced by reaction of acrylic acid with hydrogen chloride and phosgene in the presence of, for example, dimethylformamide as catalyst, or by reaction of propiolactone with thionyl chloride.

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View Lastest Price from 3-Chloropropionyl chloride manufacturers

Henan Fengda Chemical Co., Ltd
Product
3-Chloropropionyl chloride 625-36-5
Price
US $8.00-0.80/KG
Min. Order
1KG
Purity
99%
Supply Ability
g-kg-tons, free sample is available
Release date
2024-01-22
R&D Scientific Inc.
Product
3-Chloropropionyl Chloride 625-36-5
Price
US $140.00/Kg
Min. Order
1Kg
Purity
99 %
Supply Ability
500 Kg
Release date
2024-03-02
Hebei Guanlang Biotechnology Co,.LTD
Product
Allylbenzene 625-36-5
Price
US $9.10/KG
Min. Order
1KG
Purity
99.%
Supply Ability
10 ton
Release date
2021-08-18

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