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CAS

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910443-26-4

6-(3,4-DICHLOROPHENYL)IMIDAZO[2,1-B][1,3]THIAZOLE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 910443-26-4 Structure

  • Basic information

    1. Product Name: 6-(3,4-DICHLOROPHENYL)IMIDAZO[2,1-B][1,3]THIAZOLE
    2. Synonyms: 6-(3,4-DICHLOROPHENYL)IMIDAZO[2,1-B][1,3]THIAZOLE
    3. CAS NO:910443-26-4
    4. Molecular Formula: C11H6Cl2N2S
    5. Molecular Weight: 269.14974
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 910443-26-4.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: 6-(3,4-DICHLOROPHENYL)IMIDAZO[2,1-B][1,3]THIAZOLE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-(3,4-DICHLOROPHENYL)IMIDAZO[2,1-B][1,3]THIAZOLE(910443-26-4)
    11. EPA Substance Registry System: 6-(3,4-DICHLOROPHENYL)IMIDAZO[2,1-B][1,3]THIAZOLE(910443-26-4)

  • 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: 910443-26-4(Hazardous Substances Data)

910443-26-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 910443-26-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,0,4,4 and 3 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 910443-26:
(8*9)+(7*1)+(6*0)+(5*4)+(4*4)+(3*3)+(2*2)+(1*6)=134
134 % 10 = 4
So 910443-26-4 is a valid CAS Registry Number.

910443-26-4Downstream Products

910443-26-4Relevant articles and documents

SELECTIVE LIGANDS OF HUMAN CONSTITUTIVE ANDROSTANE RECEPTOR

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Page/Page column 17-19, (2020/11/12)

The present invention provides a structurally novel class of heterocyclic compounds of general formula I wherein L1 is heteroaryl and L2 is heteroaryl or aryl. The novel compounds are useful in a method of prevention or treatment of a condition which is m

Metal-Free Aerobic Oxidative Selective C-C Bond Cleavage in Heteroaryl-Containing Primary and Secondary Alcohols

Xia, Anjie,Qi, Xueyu,Mao, Xin,Wu, Xiaoai,Yang, Xin,Zhang, Rong,Xiang, Zhiyu,Lian, Zhong,Chen, Yingchun,Yang, Shengyong

, (2019/05/07)

A transition-metal-free aerobic oxidative selective C-C bond-cleavage reaction in primary and secondary heteroaryl alcohols is reported. This reaction was highly efficient and tolerated various heteroaryl alcohols, generating a carboxylic acid derivative and a neutral heteroaromatic compound. Experimental studies combined with density functional theory calculations revealed the mechanism underlying the selective C-C bond cleavage. This strategy also provides an alternative simple approach to carboxylation reaction.

Hypervalent iodine(iii) sulfonate mediated synthesis of 6-arylimidazo[2,1-b]thiazoles in liquid PEG-400

Wu, Fang-Wen,Hou, Rei-Sheu,Wang, Huey-Min,Kang, Iou-Jiun,Chen, Ling-Ching

experimental part, p. 663 - 666 (2012/07/03)

PEG-400[poly(ethylene glycol-400)] is used as reaction medium in the one-pot synthesis of 6-arylimidazo[ 2,1-b]thiazoles by reaction with aryl ketones, hypervalent iodine(III) sulfonate and 2-aminothiazole. Significant rate enhancements and improved yield

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