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2,3-Dichloropropionyl chloride is a chemical compound with the formula C3H3Cl3O, characterized as a colorless liquid with a pungent odor. It is highly reactive, readily forming acyl chloride groups that serve as crucial intermediates in the synthesis of various chemical compounds.

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  • 7623-13-4 Structure
  • Basic information

    1. Product Name: 2,3-DICHLOROPROPIONYL CHLORIDE
    2. Synonyms: 2,3-dichloro-propanoylchlorid;Propanoyl chloride, 2,3-dichloro-;2,3-Dichloropropionic acid chloride;2,3-DICHLOROPROPIONYL CHLORIDE;2,3-Dichloropropanoyl chloride
    3. CAS NO:7623-13-4
    4. Molecular Formula: C3H3Cl3O
    5. Molecular Weight: 161.41
    6. EINECS: 231-541-2
    7. Product Categories: Acid Halides;Carbonyl Compounds;Organic Building Blocks
    8. Mol File: 7623-13-4.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 53-54 °C17 mm Hg(lit.)
    3. Flash Point: >230 °F
    4. Appearance: /
    5. Density: 1.476 g/mL at 25 °C(lit.)
    6. Vapor Pressure: 3.32mmHg at 25°C
    7. Refractive Index: n20/D 1.477(lit.)
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2,3-DICHLOROPROPIONYL CHLORIDE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2,3-DICHLOROPROPIONYL CHLORIDE(7623-13-4)
    12. EPA Substance Registry System: 2,3-DICHLOROPROPIONYL CHLORIDE(7623-13-4)
  • Safety Data

    1. Hazard Codes: C
    2. Statements: 14-35
    3. Safety Statements: 9-26-36/37/39-45
    4. RIDADR: UN 3265 8/PG 2
    5. WGK Germany: 3
    6. RTECS:
    7. F: 19-21
    8. HazardClass: 8
    9. PackingGroup: III
    10. Hazardous Substances Data: 7623-13-4(Hazardous Substances Data)

7623-13-4 Usage

Uses

Used in Pharmaceutical Industry:
2,3-Dichloropropionyl chloride is utilized as a building block for the development of new drugs, playing a vital role in the synthesis of pharmaceuticals due to its reactivity and ability to form acyl chloride groups.
Used in Agrochemical Production:
2,3-DICHLOROPROPIONYL CHLORIDE also serves as an intermediate in the production of insecticides and herbicides, contributing to the development of effective agricultural chemicals for pest and weed control.
Safety Considerations:
It is important to handle 2,3-dichloropropionyl chloride with caution due to its potential to cause irritation to the skin, eyes, and respiratory system. Moreover, its high flammability necessitates proper storage and handling in accordance with established safety protocols.

Check Digit Verification of cas no

The CAS Registry Mumber 7623-13-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,2 and 3 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7623-13:
(6*7)+(5*6)+(4*2)+(3*3)+(2*1)+(1*3)=94
94 % 10 = 4
So 7623-13-4 is a valid CAS Registry Number.
InChI:InChI=1/C3H3Cl3O/c4-1-2(5)3(6)7/h2H,1H2

7623-13-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-dichloropropanoyl chloride

1.2 Other means of identification

Product number -
Other names 2,3-Dichlor-propionylchlorid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7623-13-4 SDS

7623-13-4Relevant articles and documents

Preparation and preservation method of 2-chloro-N-n-octyl acrylamide

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Paragraph 0016; 0017, (2017/08/30)

The invention discloses a preparation and preservation method of 2-chloro-N-n-octyl acrylamide. The 2-chloro-N-n-octyl acrylamide is an impurity concomitant with production of DCOIT, and the prepared high-purity 2-chloro-N-n-octyl acrylamide has a role in guiding production of the DCOIT. The method comprises that 2,3-methyl dichloropropionate is subjected to three-step reaction of hydrolysis, acylating chlorination and amination dehydrochlorination to obtain the final product, and an antioxidant is added in purification and preservation processes and can prevent polymerization metamorphism of the product.

Reaction of (α-halogenoalkyl)thiiranes with nucleophilic reagents I. Reaction with morpholine

Tomashevskii, A. A.,Sokolov, V. V.,Potekhin, A. A.

, p. 1610 - 1618 (2007/10/03)

By means of deuterated compounds it was established that (chloromethyl)thiirane reacts with morpholine by a mechanism involving initial opening of the thiirane ring followed by recyclization.In the case of (bromomethyl)thiirane direct substitution of the bromine begins to compete with this mechanism. 2-Methyl-2-(chloromethyl)thiirane, 2,2-dimethyl-3-(chloromethyl)thiirane, and the diastereomeric (1-chloroethyl)thiiranes were synthesized, and their reactivity toward morpholine was studied.

α-FLUOROACRYLIC ACID CHLORANHYDRIDE

Boguslavskaya, L. S.,Morozova, T. V.

, p. 716 - 720 (2007/10/02)

Kinetic studies were carried out on the reaction of 2-fluoro-3-chloropropanoic acid and other halo- and methoxy-substituted propanoic acids with thionyl chloride at 50-110 deg C.The catalytic dehydro-chlorination of 2-fluoro-3-chloropropanoic acid chloranhydride by tertiary amines and their salts was investigated.Dimethylaniline chlorohydrate was shown to be an effective catalyst, providing maximum dehydrochlorination at a concentration of 20percent.A mechanism for the reaction was proposed.

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