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2,2-Dichlorobutanoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 13023-00-2 Structure
  • Basic information

    1. Product Name: 2,2-Dichlorobutanoic acid
    2. Synonyms: 2,2-Dichlorobutanoic acid;2,2-Dichlorobutyric acid
    3. CAS NO:13023-00-2
    4. Molecular Formula: C4H6 Cl2 O2
    5. Molecular Weight: 156.9952
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 13023-00-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 218.43°C (rough estimate)
    3. Flash Point: 85.7°C
    4. Appearance: /
    5. Density: 1.3890
    6. Vapor Pressure: 0.0487mmHg at 25°C
    7. Refractive Index: 1.4456 (estimate)
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2,2-Dichlorobutanoic acid(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2,2-Dichlorobutanoic acid(13023-00-2)
    12. EPA Substance Registry System: 2,2-Dichlorobutanoic acid(13023-00-2)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 13023-00-2(Hazardous Substances Data)

13023-00-2 Usage

Appearance

Colorless, odorless liquid Describes the physical appearance of the compound, which lacks color and smell and exists in a liquid state.

Solubility

Soluble in water Indicates the compound's ability to dissolve in water, making it easier to mix and apply as a pesticide or herbicide.

Common uses

Pesticide and herbicide Lists the primary applications of 2,2-Dichlorobutanoic acid, which include controlling pests and unwanted plants.

Target weeds

Broadleaf weeds Specifies the type of weeds that 2,2-Dichlorobutanoic acid is most effective in controlling, focusing on broadleaf plants.

Mode of action

Inhibition of 4-hydroxyphenylpyruvate dioxygenase Explains the compound's function in inhibiting a specific enzyme, which disrupts the biosynthesis of essential aromatic amino acids in plants.

Environmental impact

Toxic to aquatic organisms Highlights the potential negative effects of the compound on aquatic life, emphasizing the need for careful handling to minimize environmental damage.

Check Digit Verification of cas no

The CAS Registry Mumber 13023-00-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,2 and 3 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 13023-00:
(7*1)+(6*3)+(5*0)+(4*2)+(3*3)+(2*0)+(1*0)=42
42 % 10 = 2
So 13023-00-2 is a valid CAS Registry Number.
InChI:InChI=1/C4H6Cl2O2/c1-2-4(5,6)3(7)8/h2H2,1H3,(H,7,8)

13023-00-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-dichlorobutanoic acid

1.2 Other means of identification

Product number -
Other names Butyric acid,2,2-dichloro

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:13023-00-2 SDS

13023-00-2Relevant articles and documents

Total synthesis of (+)- and (-)-decursivine and (±)-serotobenine through a cascade witkop photocyclization/elimination/addition sequence: Scope and mechanistic insights

Hu, Weimin,Qin, Hua,Cui, Yuxin,Jia, Yanxing

supporting information, p. 3139 - 3147 (2013/03/28)

In this article, the total syntheses of antimalarial compound decursivine and its biologically inactive sibling serotobenine are presented. The biomimetic synthesis of (±)-serotobenine was investigated first, but failed. During the subsequent investigatio

Oxidation of aliphatic 2,2-dichloroalkanals by HNO3 in CH 2Cl2: An easy and eco-friendly route to the corresponding 2,2-dichloroalkanoic acids

Bellesia, Franco,De Buyck, Laurent,Ghelfi, Franco,Pagnoni, Ugo M.,Strazzolini, Paolo

, p. 1473 - 1481 (2007/10/03)

A simple, economically convenient, and eco-compatible procedure for the oxidation of 2,2-dichloroalkanals to the corresponding alkanoic acids has been set up, employing HNO3 in CH2O2, in the presence of NaNO2 as catalyst.

2,2-dichloroaldehydes and 2,2-dichlorocarboxylic acids from 2- picoline·HCl catalyzed chlorination of aldehydes

Bellesia, Franco,De Buyck, Laurent,Ghelfi, Franco

, p. 146 - 148 (2007/10/03)

An efficient preparation of 2,2-dichloroaldehydes and 2,2- dichlorocarboxylic acids has been achieved by chlorination of aldehydes using 2-picoline hydrochloride as recoverable catalyst.

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