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CAS

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126006-79-9

2-[(biphenyl-4-yloxy)acetyl]-N-(2,4-dimethylphenyl)hydrazinecarbothioamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 126006-79-9 Structure

  • Basic information

    1. Product Name: 2-[(biphenyl-4-yloxy)acetyl]-N-(2,4-dimethylphenyl)hydrazinecarbothioamide
    2. Synonyms:
    3. CAS NO:126006-79-9
    4. Molecular Formula: C23H23N3O2S
    5. Molecular Weight: 405.5126
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 126006-79-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: 1.236g/cm3
    6. Refractive Index: 1.653
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-[(biphenyl-4-yloxy)acetyl]-N-(2,4-dimethylphenyl)hydrazinecarbothioamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-[(biphenyl-4-yloxy)acetyl]-N-(2,4-dimethylphenyl)hydrazinecarbothioamide(126006-79-9)
    11. EPA Substance Registry System: 2-[(biphenyl-4-yloxy)acetyl]-N-(2,4-dimethylphenyl)hydrazinecarbothioamide(126006-79-9)

  • 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: 126006-79-9(Hazardous Substances Data)

126006-79-9 Usage

Molecular structure

The compound has a complex molecular structure that includes a biphenyl-4-yloxy group, a 2,4-dimethylphenyl group, and a hydrazinecarbothioamide group.

Pharmacological properties

The compound has potential pharmaceutical properties and has been studied for its potential use in the treatment of various diseases and conditions.

Derivative of hydrazinecarbothioamide

The compound is a derivative of hydrazinecarbothioamide, which may contribute to its biological activity.

Acetyl derivative

The compound is an acetyl derivative, suggesting that it may have a role in modulating certain cellular processes.

Further research needed

Further research is needed to fully understand the potential applications of 2-[(biphenyl-4-yloxy)acetyl]-N-(2,4-dimethylphenyl)hydrazinecarbothioamide.

Check Digit Verification of cas no

The CAS Registry Mumber 126006-79-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,0,0 and 6 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 126006-79:
(8*1)+(7*2)+(6*6)+(5*0)+(4*0)+(3*6)+(2*7)+(1*9)=99
99 % 10 = 9
So 126006-79-9 is a valid CAS Registry Number.

126006-79-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2,4-dimethylphenyl)-3-[[2-(4-phenylphenoxy)acetyl]amino]thiourea

1.2 Other means of identification

Product number -
Other names ((1,1'-Biphenyl)-4-yloxy)acetic acid 2-(((2,4-dimethylphenyl)amino)thioxomethyl)hydrazide

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:126006-79-9 SDS

126006-79-9Relevant articles and documents

1,3,4-Oxadiazole/thiadiazole and 1,2,4-triazole derivatives of biphenyl-4-yloxy acetic acid: Synthesis and preliminary evaluation of biological properties

Kumar, Harish,Javed, Sadique A.,Khan, Suroor A.,Amir, Mohammad

experimental part, p. 2688 - 2698 (2009/04/11)

A series of 1,3,4-oxadiazole/thiadiazole and 1,2,4-triazole derivatives of biphenyl-4-yloxy acetic acid were synthesized in order to obtain new compounds with potential anti-inflammatory activity, analgesic activity and lower ulcerogenic potential. All co

Anti-inflammatory activity of substituted 1,3,4-oxadiazoles

Raman,Parmar,Salzman

, p. 999 - 1002 (2007/10/02)

Various 2-(4-biphenoxymethyl)-5-arylamino-1,3,4-oxadiazoles were synthesized by cyclization of the corresponding 1-(4-biphenoxyacetyl)-4-substituted thiosemicarbazides. These compounds were characterized by their elemental analyses and infrared, mass, and

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