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2,5-Dichlorothiobenzamide, with the molecular formula C7H5Cl2NOS, is a white to light yellow crystalline solid. It is a chemical compound primarily utilized as an intermediate in the synthesis of various chemicals and pharmaceuticals. Due to its chemical properties, it is also employed as a raw material in the production of pesticides and herbicides. However, it is recognized as a skin and eye irritant, necessitating careful handling and adherence to safety protocols to avoid potential health risks.

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  • 69622-81-7 Structure
  • Basic information

    1. Product Name: 2,5-DICHLOROTHIOBENZAMIDE
    2. Synonyms: Benzamide,2,5-dichlorothio- (7CI)
    3. CAS NO:69622-81-7
    4. Molecular Formula: C7H5Cl2NS
    5. Molecular Weight: 206.09
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 69622-81-7.mol
  • Chemical Properties

    1. Melting Point: 88-92℃
    2. Boiling Point: 322.3°C at 760 mmHg
    3. Flash Point: 148.7°C
    4. Appearance: /
    5. Density: 1.473g/cm3
    6. Vapor Pressure: 0.000282mmHg at 25°C
    7. Refractive Index: 1.669
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2,5-DICHLOROTHIOBENZAMIDE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2,5-DICHLOROTHIOBENZAMIDE(69622-81-7)
    12. EPA Substance Registry System: 2,5-DICHLOROTHIOBENZAMIDE(69622-81-7)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: 6.1
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 69622-81-7(Hazardous Substances Data)

69622-81-7 Usage

Uses

Used in Chemical and Pharmaceutical Industries:
2,5-Dichlorothiobenzamide is used as an intermediate in the synthesis of various chemical compounds and pharmaceuticals for its ability to contribute to the formation of complex molecules required in these industries.
Used in Pesticide and Herbicide Production:
2,5-Dichlorothiobenzamide is used as a raw material in the production of pesticides and herbicides, where its chemical properties are leveraged to create effective agents for controlling pests and unwanted plant growth.

Check Digit Verification of cas no

The CAS Registry Mumber 69622-81-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,6,2 and 2 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 69622-81:
(7*6)+(6*9)+(5*6)+(4*2)+(3*2)+(2*8)+(1*1)=157
157 % 10 = 7
So 69622-81-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H5Cl2NS/c8-4-1-2-6(9)5(3-4)7(10)11/h1-3H,(H2,10,11)

69622-81-7 Well-known Company Product Price

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  • Alfa Aesar

  • (H32323)  2,5-Dichlorothiobenzamide, 97%   

  • 69622-81-7

  • 250mg

  • 428.0CNY

  • Detail
  • Alfa Aesar

  • (H32323)  2,5-Dichlorothiobenzamide, 97%   

  • 69622-81-7

  • 1g

  • 1186.0CNY

  • Detail

69622-81-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5-dichlorobenzenecarbothioamide

1.2 Other means of identification

Product number -
Other names Benzamide,2,5-dichlorothio-(7CI)

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:69622-81-7 SDS

69622-81-7Relevant articles and documents

Optimizing thiadiazole analogues of resveratrol versus three chemopreventive targets

Mayhoub, Abdelrahman S.,Marler, Laura,Kondratyuk, Tamara P.,Park, Eun-Jung,Pezzuto, John M.,Cushman, Mark

experimental part, p. 510 - 520 (2012/03/10)

Chemoprevention is an approach to decrease cancer morbidity and mortality through inhibition of carcinogenesis and prevention of disease progression. Although the trans stilbene derivative resveratrol has chemopreventive properties, its action is compromised by weak non-specific effects on many biological targets. Replacement of the stilbene ethylenic bridge of resveratrol with a 1,2,4-thiadiazole heterocycle and modification of the substituents on the two aromatic rings afforded potential chemopreventive agents with enhanced potencies and selectivities when evaluated as inhibitors of aromatase and NF-κB and inducers of quinone reductase 1 (QR1).

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