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7124-53-0

Carbonodithioic acid, ortho-butyls-2-propenylester, also known as 2-Propenyl carbonodithioic acid, o-butyl ester, is a chemical compound with the molecular formula C7H12S2. It is an organosulfur compound that belongs to the class of dithiocarbamates, which are widely used as fungicides, herbicides, and vulcanization accelerators in the rubber industry. This specific compound is characterized by the presence of a dithiocarbamate group (-S2C-NH-) attached to a 2-propenyl (allyl) group and an ortho-butyl group. It is a colorless to pale yellow liquid with a pungent odor and is soluble in organic solvents. Due to its reactivity and potential toxicity, it is important to handle this chemical with care and follow proper safety precautions.

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  • 7124-53-0 Structure

  • Basic information

    1. Product Name: CARBONODITHIOICACID,ORTHO-BUTYLS-2-PROPENYLESTER
    2. Synonyms: CARBONODITHIOICACID,ORTHO-BUTYLS-2-PROPENYLESTER
    3. CAS NO:7124-53-0
    4. Molecular Formula: C8H14OS2
    5. Molecular Weight: 190.32616
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 7124-53-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: CARBONODITHIOICACID,ORTHO-BUTYLS-2-PROPENYLESTER(CAS DataBase Reference)
    10. NIST Chemistry Reference: CARBONODITHIOICACID,ORTHO-BUTYLS-2-PROPENYLESTER(7124-53-0)
    11. EPA Substance Registry System: CARBONODITHIOICACID,ORTHO-BUTYLS-2-PROPENYLESTER(7124-53-0)

  • 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: 7124-53-0(Hazardous Substances Data)

7124-53-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7124-53-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,2 and 4 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7124-53:
(6*7)+(5*1)+(4*2)+(3*4)+(2*5)+(1*3)=80
80 % 10 = 0
So 7124-53-0 is a valid CAS Registry Number.

7124-53-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name O-butyl prop-2-enylsulfanylmethanethioate

1.2 Other means of identification

Product number -
Other names Dithiokohlensaeure-S-allylester-O-butylester

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:7124-53-0 SDS

7124-53-0Downstream Products

7124-53-0Relevant articles and documents

Preparation method of xanthate compound

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Paragraph 0037; 0038; 0039; 0040, (2020/11/05)

The invention discloses a preparation method of an xanthate compound. The method is characterized in that an xanthate and a chloride react at 0-60 DEG C in the presence of a phase transfer catalyst toprepare the xanthate compound with high purity and high yield. Compared with the existing method, the process for preparing xanthate compounds by phase transfer catalysis without solvent (self-solvent) is simple, the product purity is good, the yield is high, and the method is economic and environment-friendly and is suitable for industrial production.

Alkyl xanthic sour alkene propyl ester compound of preparation method (by machine translation)

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Paragraph 0025, (2017/03/17)

The invention discloses a alkyl xanthic sour alkene propyl ester compound of preparation method. A alkyl xanthic sour alkene propyl ester compound of preparation method, used for preparing alkyl xanthogen ally propyl ester dressing agent. Characterized in that a safe, non-corrosive to the allylic alcohol compound alternative flammable, extremely volatile allyl chlorine apperception compound as raw material, with the alkyl xanthic acid salt reaction for preparing alkyl xanthogen ally propyl ester compounds, through the liquid, washing, and drying to obtain alkyl xanthic sour alkene terephthalate, thus make the production process more environmental protection, security. (by machine translation)

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